Chemical Engineer Jobs in Morocco

<p><b>Job Description</b></p><p>Regulatory Knowledge &amp; Compliance</p><p>Strong understanding of EU regulations (REACH, ELV, SCIP) and company policies. Ability to assess and ensure compliance of materials and parts with regulatory requirements.</p><p>Chemical &amp; Material Science Expertise</p><p>Knowledge of chemical substances, their impact, and potential replacements. Experience in material assessment and elimination of regulated substances.</p><p>Data Management &amp; Analytical Skills</p><p>Ability to collect, analyze, and assess IMDS/MSDS data for compliance. Conduct impact analysis and monitor the authorization process for substances.</p><p>Supplier &amp; Stakeholder Coordination</p><p>Experience in conducting supplier surveys and evaluating their chemical management processes. Strong communication and negotiation skills to ensure timely responses.</p><p>Problem-Solving &amp; Process Improvement</p><p>Ability to develop and execute action plans for eliminating regulated substances. Continuous improvement mindset for optimizing workflows and adapting to new tools.</p><p>Attention to Detail &amp; Quality Assurance</p><p>Ensuring accuracy in regulatory documentation, design updates, and supplier evaluations. Commitment to maintaining high standards in engineering and compliance tasks.</p><p><strong>Desired Candidate Profile</strong></p><p>Qualifications</p><p>1 to 5 Years of a experience in product compliance, regulatory affairs, or material assessment in automotive, aerospace, or manufacturing industries</p><p>Profeciency level in both french and english</p><p>Master s degree in one of the following fields: Mechanical Engineering, Material Science &amp; Engineering, Chemical Engineering, or Automotive or Aerospace Engineering</p><p>Good Knowledge of EU regulations (REACH)</p>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br> Company culture : <p><strong>Alten Maroc </strong>is defined by a deeply <strong>collaborative</strong> culture, focused on people, trust, and strong team support, with hands-on managers who guide and develop talent.<br> This environment is enhanced by a strong drive for <strong>innovation</strong>, encouraging creativity, initiative, and experimentation across projects.<br> A structured and disciplined organization ensures <strong>efficiency</strong>, rigor, and quality in engineering delivery.<br> <strong>Performance</strong> and ambition are part of the culture as well, supporting collective success while maintaining a positive and caring atmosphere. </p><br><br> <br> Job : <p><strong>Regulatory Knowledge &amp; Compliance</strong></p><br><br><ul><li>Strong understanding of EU regulations (REACH, ELV, SCIP) and company policies.</li><li>Ability to assess and ensure compliance of materials and parts with regulatory requirements.</li></ul><p><strong>Chemical &amp; Material Science Expertise</strong></p><br><br><ul><li>Knowledge of chemical substances, their impact, and potential replacements.</li><li>Experience in material assessment and elimination of regulated substances.</li></ul><p><strong>Data Management &amp; Analytical Skills</strong></p><br><br><ul><li>Ability to collect, analyze, and assess IMDS/MSDS data for compliance.</li><li>Conduct impact analysis and monitor the authorization process for substances.</li></ul><p><strong>Supplier &amp; Stakeholder Coordination</strong></p><br><br><ul><li>Experience in conducting supplier surveys and evaluating their chemical management processes.</li><li>Strong communication and negotiation skills to ensure timely responses.</li></ul><p><strong>Problem-Solving &amp; Process Improvement</strong></p><br><br><ul><li>Ability to develop and execute action plans for eliminating regulated substances.</li><li>Continuous improvement mindset for optimizing workflows and adapting to new tools.</li></ul><p><strong>Attention to Detail &amp; Quality Assurance</strong></p><br><br><ul><li>Ensuring accuracy in regulatory documentation, design updates, and supplier evaluations.</li><li>Commitment to maintaining high standards in engineering and compliance tasks.</li></ul> <br> Required profile : <ul><li>1 to 5 Years of experience in product compliance, regulatory affairs, or material assessment in automotive, aerospace, or manufacturing industries</li><li>Proficiency level in both French and English</li><li>Master's degree in one of the following fields: Mechanical Engineering, Material Science &amp; Engineering, Chemical Engineering, or Automotive or Aerospace Engineering</li><li>Good Knowledge of EU regulations (REACH)</li></ul> <br><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><strong>Location:</strong> Casablanca, Morocco</p><br><p><strong>Job Type:</strong> Full-time</p><br><p><strong>Hashtag:</strong> #LI-MM1</p><br><p><strong>About Us </strong></p><br><p>For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</p><br><p>As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.&nbsp;</p><br><p><strong>Description:</strong></p><br><p>We are looking for a talented<strong>, Sr. Supervisor, Formulation Development</strong>to join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</p><br><p>If you want to be part of a team that cares about impact, this is the place for you.</p><br><p><strong>Key Responsibilities:</strong></p><br><ul><li>Lead technology transfer activities from R&amp;D to manufacturing.</li><li>Oversee process optimization and scale-up activities.</li><li>Plan and manage development projects, timelines, resources, and budgets.</li><li>Work closely with R&amp;D, PMO, Quality Assurance, Production, Regulatory Affairs, and Supply Chain.</li><li>Lead, coach, and develop a team of formulation development professionals.</li><li>Ensure accurate documentation and compliance with cGMP and regulatory requirements.</li></ul><p><strong>Qualifications:</strong></p><br><p>We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</p><br><ul><li>Degree in Pharmacy, Chemical Engineering, or a related field.</li><li>5 to 10 years of experience in pharmaceutical manufacturing or industrial development.</li><li>Experience in technology transfer, process scale-up, and cross-functional project management.</li><li>Strong knowledge of GMP and regulatory requirements.</li><li>Good communication, analytical, and leadership skills.</li><li>Fluent in English and French</li></ul> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Job : <p>Key Responsibilities</p><br><br><p>EHS System Management: Deploy, maintain, and improve the EHS management system in accordance with ISO standards (14001, 45001, 50001) and Group guidelines.</p><br><br><p>Compliance &amp; Regulatory Affairs: Ensure strict adherence to the Moroccan Labor Code (Law 65-99) and environmental laws. Act as the primary liaison with local authorities (labor inspectors, fire departments, environmental regulators).</p><br><br><p>Risk Management &amp; Operational Safety: Assess and mitigate risks related to chemicals, machinery, and working at heights. Supervise the safety of employees and subcontractors during both construction and production phases.</p><br><br><p>Environmental Management: Oversee the compliant disposal of waste (especially hazardous and chemical waste), monitor emissions (VOCs, wastewater), and contribute to sustainability goals (ESG, carbon footprint).</p><br><br><p>Incident &amp; Emergency Management: Lead investigations following accidents or near misses, implement corrective actions, and maintain fire protection systems and emergency response plans.</p><br><br><p>Culture &amp; Team Building: Recruit and manage a local EHS team, audit suppliers, and establish a proactive safety culture across all levels of the plant.</p><br><br> <br> Required profile : <p>Candidate Profile</p><br><br><p>Education: Bachelor's degree minimum (Master's preferred) in Safety Engineering, Environmental Engineering, Occupational Health, or Chemical Engineering.</p><br><br><p>Experience: At least 5 years of EHS management experience in the industrial sector, including a minimum of 2 years in a Manager or leadership role.</p><br><br><p>Industry Background: Required experience in demanding industrial environments (chemicals, automotive, battery manufacturing, or large-scale construction projects).</p><br><br><p>Technical Expertise: Proven mastery of ISO 14001 and 45001 standards as well as the Moroccan legal framework. An international certification (NEBOSH, IOSH) is a strong asset.</p><br><br><p>Multicultural Environment: Prior experience within an international or Asian/Chinese company is highly valued to facilitate management synergies and cross-cultural communication.</p><br><br><p>Languages: Perfect fluency in French or Arabic (for interactions with local authorities and shop-floor operations) AND a good level of English (written and spoken) for corporate Group reporting.</p><br><br><p>Soft Skills: Strong leadership, adaptability to simultaneously manage a construction site and an operational start-up, and excellent coordination abilities.</p><br><br> <br><br> </div>

<p><br></p> <h4><b>YOUR ROLE</b></h4> <p>osition summary The Environmental Engineer is responsible for implementing and maintaining environmental management programs in an industrial setting. The role ensures compliance with environmental legislation, corporate standards, and site objectives related to emissions, waste, water, energy, chemical handling, and pollution prevention. A key part of the role is assessing chemical-related environmental aspects and risks.</p> <h4><b><br></b></h4><h4><b>Main responsibilities</b></h4> <ul> <li>Ensure compliance with applicable environmental laws, regulations, permits, and company standards</li> <li>Identify, assess, and monitor environmental impacts related to industrial operations</li> <li>Conduct environmental risk assessments, including chemical storage, handling, use, transport, and disposal</li> <li>Review chemical inventories, Safety Data Sheets, and associated environmental hazards</li> <li>Evaluate risks related to air emissions, wastewater, waste generation, soil contamination, and accidental releases</li> <li>Support environmental permits, reporting, inspections, and audits</li> <li>Develop and track environmental KPIs, action plans, and improvement initiatives</li> <li>Monitor waste management, recycling, hazardous waste segregation, and disposal contractors</li> <li>Support water management, energy-saving initiatives, and pollution prevention projects</li> <li>Participate in incident investigations involving environmental spills, leaks, or chemical releases</li> <li>Coordinate corrective and preventive actions with operations, maintenance, HSE, and suppliers</li> <li>Deliver environmental awareness and chemical handling training to employees and contractors</li> <li>Support emergency preparedness and response for chemical or environmental incidents</li> <li>Maintain environmental documentation, records, and regulatory reporting</li> </ul> <h4>Chemical assessment responsibilities</h4> <ul> <li>Perform environmental impact assessments for chemicals used on site</li> <li>Review compatibility, storage conditions, containment, and labeling requirements</li> <li>Assess substitution opportunities for less hazardous or more sustainable alternatives</li> <li>Verify disposal methods for chemical waste and contaminated materials</li> <li>Ensure chemical use complies with internal approval processes and regulatory requirements</li> <li>Support exposure and release prevention measures in coordination with safety teams</li> </ul><p><strong>Desired Candidate Profile</strong></p><p>YOUR SKILLS &amp; EXPERIENCES</p> <ul> <li>Engineer/ Master degree in Environmental Engineering, Chemical Engineering, Industrial Engineering, or a related field</li> <li>Experience in an industrial or manufacturing environment</li> <li>Knowledge of environmental legislation, chemical risk assessment, and waste management</li> <li>Understanding of emissions control, wastewater, hazardous substances, and spill prevention</li> <li>Strong analytical and reporting skills</li> <li>Experience with ISO 14001 or integrated management systems</li> <li>Familiarity with chemical regulatory frameworks and SDS interpretation</li> <li>Good project management and problem-solving abilities</li> <li>Strong communication skills and ability to influence cross-functional teams</li> <li>Proficiency in environmental data tracking and reporting tools</li> <li>Detail-oriented and structured</li> <li>Proactive and solution-oriented</li> <li>Strong teamwork and stakeholder management</li> <li>Able to work under pressure and manage priorities</li> <li>Committed to continuous improvement and sustainability</li> </ul>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><b>Use Your Power for Purpose</b></p><br><br><p>Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.</p><br><br><p><b>What You Will Achieve</b></p><br><br><p>In this role, you will:</p><br><br><ul><li>Develop and maintain qualification and validation strategies.</li><li>Support the update of the Site Validation Master Plan.</li><li>Prepare, execute, and review qualification and validation documentation.</li><li>Coordinate cleaning validation activities, including protocol preparation, report issuance, and runs scheduling.</li><li>Coordinate process validation and holding time validation activities.</li><li>Track qualification and validation schedules to ensure timely completion.</li><li>Participate in periodic requalification and qualified state assessments of equipment and utilities.</li><li>Create, revise, and maintain GMP documentation under QA responsibility.</li><li>Participate in investigations related to qualification and validation anomalies.</li><li>Contribute to the preparation and revision of procedures related to qualified equipment and validated processes.</li><li>Support deviation, change control, and CAPA processes, including impact assessments and effectiveness follow-up until closure.</li><li>Act as backup for the Quality System Specialist when required.</li><li>Support QA departmental activities, KPI monitoring, compliance initiatives, and continuous improvement programs.</li></ul><br><p><b>Here Is What You Need (Minimum Requirements)</b></p><br><br><ul><li>Pharmacist, master’s degree, or equivalent qualification in Pharmacy, Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Quality Assurance, or a related scientific discipline.</li><li>Minimum of 3 years Experience in the pharmaceutical industry, Quality Assurance.</li><li>Sound knowledge of current Good Manufacturing Practices (part of GxP)</li><li>Ability to work effectively in a team environment, both within one's own team and interdepartmental teams.</li><li>Effective written and oral communication skills.</li></ul><br><p><b>Bonus Points If You Have (Preferred Requirements)</b></p><br><br><ul><li>Experience at a manufacturing site.</li><li>Master's specialization in Pharmaceutical Quality Assurance is preferred.</li><li>Experience in qualification, validation, deviation management, change control, CAPA management, and GMP documentation.</li><li>Experience supporting continuous improvement and GMP training initiatives.</li><li>Strong problem-solving skills.</li><li>Ability to work independently and as part of a team.</li><li>Excellent time management and multitasking abilities.</li><li>Experience using common AI tools, including generative technologies such&nbsp;as ChatGPT or Microsoft Copilot, to support problem solving and enhancement.</li></ul> <br>Work Location Assignment: On Premise<br><br><p><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><br><br><br><br><p>To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on&nbsp;<span><u>Pfizer Careers</u></span>.</p><br><br>&amp;#xa;Quality Assurance and Control<br><br><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision spending your summer working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for participants in the Technical Development Program Internship at AbbVie Bioresearch Center (ABC) in Worcester, MA. </p><br><p><u><strong>Technical Development Program Internship Description:</strong></u></p><br><p>As a Technical Development Program intern, you will participate in a paid, 11-week summer program working on meaningful assignments that have a real impact on our business and patients worldwide. </p><br><p><strong>Past examples of projects have included:&nbsp;</strong></p><br><ul><li><p>Product and process optimization in a manufacturing facility&nbsp;</p><br></li></ul><ul><li><p>Quality systems data analysis to identify compliance trends&nbsp;</p><br></li></ul><ul><li><p>EHS risk management assessment </p><br></li></ul><p>AbbVie offers you an opportunity for potential work experiences that are aligned to a variety of functional areas, including those listed below. Interns will be placed in assignments based on business needs and skill set. </p><br><ul><li><p>Manufacturing&nbsp;</p><br></li></ul><ul><li><p>Engineering&nbsp;</p><br></li></ul><ul><li><p>Supply Chain&nbsp;</p><br></li></ul><p>ABC strongly considers high performing interns as candidates for our Technical Development Program (TDP) after they graduate. ABC’s TDP is a three-year rotational program with three separate work assignments. The rotations are carried out in a variety of functional areas within Operations. The goal of the program is to develop AbbVie’s future leaders, provide exposure across the business functions, and forums for skill and professional development.&nbsp;</p><br><br>Qualifications<br><br><p><u><strong>Minimum Qualifications:&nbsp;</strong></u></p><br><ul><li><p>Must be currently enrolled in university, pursuing a bachelor's degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, or related major.&nbsp;</p><br></li></ul><ul><li><p>Must be enrolled in university the semester following your internship&nbsp;</p><br></li></ul><ul><li><p>Expected graduation date between December 2027&nbsp;and May 2028&nbsp;</p><br></li></ul><ul><li><p>Demonstrated leadership skills (i.e., extracurricular activities or projects) </p><br></li></ul><p><u><strong>Preferred Qualifications:&nbsp;</strong></u></p><br><ul><li><p>Excellent problem-solving, written, and verbal skills </p><br></li></ul><ul><li><p>Exceptional interpersonal, leadership and project management skills </p><br></li></ul><ul><li><p>Proven track record of teamwork, adaptability, innovation, initiative, and integrity</p><br></li></ul><br>Additional Information<br><br><p>Benefits and Amenities:<br>Competitive pay<br>Relocation support for eligible students<br>Select wellness benefits and paid holiday / sick time<br>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​<br>​The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​<br>​<br>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision spending 6 months working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie AbbVie Co-Ops. </p><br><p>The Quality Assurance Validation department is responsible for plant validation including validated system (Equipment/Process), risk/design and change control compliance. Our team ensures alignment with Global Quality Systems for validation and related functions, e.g. engineering, risk management.&nbsp;</p><br><p><strong>Key responsibilities include:&nbsp;</strong></p><br><p>The Validation Engineering&nbsp;Co-Op&nbsp;will support the planning and execution of tasks reporting into the QA Validation department. This role will support various areas of manufacturing and/or Quality Control (QC) and interact heavily with our quality organization. Expectations of the role include:&nbsp;</p><br><ul><li><p>&nbsp;Execute task as required to implement the Validation Master Plan&nbsp;</p><br></li></ul><ul><li><p>&nbsp;Participate with external engineering and QC departments on new installations, system modifications and decommissioning&nbsp;</p><br></li></ul><ul><li><p>&nbsp;Draft and execute validation plans, and validation protocols in compliance with cGMP practices&nbsp;</p><br></li></ul><ul><li><p>&nbsp;Ensures investigations of validation failures are completed thoroughly and documented accurately&nbsp;</p><br></li></ul><br>Qualifications<br><br><p><strong>Basic Qualifications&nbsp;</strong></p><br><ul><li><p>Currently enrolled in university, pursuing a Bachelor’s in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering&nbsp;or other related field&nbsp;</p><br></li></ul><ul><li><p>Must be enrolled in university for at least one semester following the co-op </p><br></li></ul><ul><li><p>Expected graduation date between&nbsp;May 2028 –&nbsp;Dec&nbsp;2028&nbsp;</p><br></li></ul><ul><li><p>Organization, attention to detail, communication, self-starter, ability to ask questions, time management, etc.&nbsp;</p><br></li></ul><ul><li><p>Experience working in Microsoft Suite, especially Excel, Word, PowerPoint&nbsp;</p><br></li></ul><ul><li><p>Must be able to commit to a 6-month duration in-person at AbbVie Bioresearch Center (ABC) in Worcester, MA (July - December).&nbsp;</p><br></li></ul><p><strong>Preferred Qualifications&nbsp;</strong></p><br><ul><li><p>Equipment-based or instrumentation / installation project exposure a plus&nbsp;</p><br></li></ul><br>Additional Information<br><br><p><strong>Benefits and Amenities:</strong><br>Competitive pay<br>Relocation support for eligible students<br>Select wellness benefits and paid holiday / sick time<br><strong>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​</strong><br>​The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​<br>​<br>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision spending 6 months working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie AbbVie Co-Ops.</p><br><p>The Quality Assurance Validation department is responsible for plant validation including validated system (Equipment/Process), risk/design and change control compliance. Our team ensures alignment with Global Quality Systems for validation and related functions, e.g. engineering, risk management.</p><br><p><strong>Key responsibilities include:</strong></p><br><p>The Validation Engineering Co-Op will support the planning and execution of tasks reporting into the QA Validation department. This role will support various areas of manufacturing and/or Quality Control (QC) and interact heavily with our quality organization. Expectations of the role include:</p><br><ul><li>&nbsp;Execute task as required to implement the Validation Master Plan</li><li>&nbsp;Participate with external engineering and QC departments on new installations, system modifications and decommissioning</li><li>&nbsp;Draft and execute validation plans, and validation protocols in compliance with cGMP practices</li><li>&nbsp;Ensures investigations of validation failures are completed thoroughly and documented accurately</li><li>Must be able to commit to a 6-month duration in-person at AbbVie Bioresearch Center (ABC) in Worcester, MA (January - July).&nbsp;</li></ul><br>Qualifications<br><br><p><strong>Basic Qualifications</strong></p><br><ul><li>Currently enrolled in university, pursuing a Bachelor’s in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering&nbsp;or other related field</li><li>Must be enrolled in university for at least one semester following the co-op&nbsp;</li><li>Expected graduation date between December 2027 – June 2028&nbsp;</li><li>Organization, attention to detail, communication, self-starter, ability to ask questions, time management, etc.</li><li>Experience working in Microsoft Suite, especially Excel, Word, PowerPoint</li></ul><p><strong>Preferred Qualifications</strong></p><br><ul><li>Equipment-based or instrumentation / installation project exposure a plus</li></ul><br>Additional Information<br><br><p><strong>Benefits and Amenities:</strong><br>Competitive pay<br>Relocation support for eligible students<br>Select wellness benefits and paid holiday / sick time<br><strong>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​</strong><br>​The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​<br>​<br>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision spending time working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie’s Co-Op's.</p><br><p>Engineering supports and enables all functions throughout the facility by operating the building utilities and control systems, maintaining the entire facility, providing technical support, managing capital projects, qualifying systems, and providing drafting support.</p><br><p><strong>Core Job Responsibilities &amp; Deliverables</strong></p><br><p>The Reliability Engineer Co-Op position reports to the Reliability&nbsp;Engineer or&nbsp;Reliability&nbsp;Manager&nbsp;and&nbsp;is responsible for:&nbsp;</p><br><ul><li>Utilizing our Computerized Maintenance Management System (CMMS) to direct the strategy and execution of facility systems, predictive and preventive maintenance.</li><li>Supporting the development, execution, and maintenance of the site,&nbsp;asset reliability program, and associated projects. </li><li>Supporting reliability and engineering tools&nbsp;such as Life-Cycle costing, Pareto, and Root Cause Failure Analysis.&nbsp;</li><li>Applying predictive maintenance technologies such as Ultrasound and Vibration analysis on a variety of equipment and systems to identify potential equipment failures and recommend the appropriate corrective action. </li></ul><ul><li>Supporting the site reliability program including asset criticality,&nbsp;maintenance strategy&nbsp;and critical spare&nbsp;parts. </li></ul><ul><li>Working with maintenance and inventory personnel in development of asset critical spare&nbsp;parts&nbsp;strategy&nbsp;and continuous improvement efforts.&nbsp;</li></ul><ul><li>Working closely with Project Engineering, Controls Engineering, Site Operations,&nbsp;and&nbsp;Maintenance&nbsp;to fulfill primary job responsibilities, and will regularly interface with site engineering management&nbsp;regarding&nbsp;the status of the Reliability program.&nbsp;</li></ul><ul><li>Supporting&nbsp;Asset Maintenance Plan to ensure adequate levels of sustaining effective maintenance&nbsp;job plans&nbsp;and critical spare parts&nbsp;for each plant&nbsp;asset.&nbsp;</li></ul><ul><li>Supporting&nbsp;Reliability Engineer as&nbsp;needed.&nbsp;</li></ul><br>Qualifications<br><br><p><strong>Minimum&nbsp;Qualifications </strong></p><br><ul><li>Currently enrolled in university, pursing a bachelor's degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or other related field.</li><li>Must be enrolled in university for at least one semester following the co-op</li><li>Expected graduation date between December 2027 – June 2028</li><li>Must be able to commit to a 6-month duration in-person at AbbVie Bioresearch Center (ABC) in Worcester, MA (January - June).</li></ul><p><strong>Preferred Qualifications</strong></p><br><ul><li>Strong communication, adaptability, networking, and creative problem-solving skills</li><li>Exposure to computerized maintenance management and business systems, including Maximo, SAP, and SharePoint</li></ul><br>Additional Information<br><br><p><strong>Benefits and Amenities:</strong><br>Competitive pay<br>Relocation support for eligible students<br>Select wellness benefits and paid holiday / sick time<br><strong>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​</strong><br>​The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​<br><strong>​</strong><br>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision spending time working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie’s Co-Op's. </p><br><p>Engineering supports and enables all functions throughout the facility by operating the building utilities and control systems, maintaining the entire facility, providing technical support, managing capital projects, qualifying systems, and providing drafting support.&nbsp;</p><br><p><strong>Core Job Responsibilities &amp; Deliverables&nbsp;</strong></p><br><p>The Reliability Engineer Co-Op position reports to the Reliability Engineer or Reliability Manager and is responsible for: </p><br><ul><li><p>Utilizing our Computerized Maintenance Management System (CMMS) to direct the strategy and execution of facility systems, predictive and preventive maintenance.&nbsp;</p><br></li></ul><ul><li><p>Supporting the development, execution, and maintenance of the site,&nbsp;asset reliability program, and associated projects. </p><br></li></ul><ul><li><p>Supporting reliability and engineering tools&nbsp;such as Life-Cycle costing, Pareto, and Root Cause Failure Analysis. </p><br></li></ul><ul><li><p>Applying predictive maintenance technologies such as Ultrasound and Vibration analysis on a variety of equipment and systems to identify potential equipment failures and recommend the appropriate corrective action. </p><br></li></ul><ul><li><p>Supporting the site reliability program including asset criticality,&nbsp;maintenance strategy&nbsp;and critical spare&nbsp;parts. </p><br></li></ul><ul><li><p>Working with maintenance and inventory personnel in development of asset critical spare&nbsp;parts&nbsp;strategy&nbsp;and continuous improvement efforts. </p><br></li></ul><ul><li><p>Working closely with Project Engineering, Controls Engineering, Site Operations,&nbsp;and&nbsp;Maintenance&nbsp;to fulfill primary job responsibilities, and will regularly interface with site engineering management&nbsp;regarding&nbsp;the status of the Reliability program. </p><br></li></ul><ul><li><p>Supporting&nbsp;Asset Maintenance Plan to ensure adequate levels of sustaining effective maintenance&nbsp;job plans&nbsp;and critical spare parts&nbsp;for each plant&nbsp;asset. </p><br></li></ul><ul><li><p>Supporting&nbsp;Reliability Engineer as&nbsp;needed.&nbsp;</p><br></li></ul><br>Qualifications<br><br><p><strong>Minimum&nbsp;Qualifications </strong></p><br><ul><li><p>Currently enrolled in university, pursing a bachelor's degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or other related field. </p><br></li></ul><ul><li><p>Must be enrolled in university for at least one semester following the co-op&nbsp;</p><br></li></ul><ul><li><p>Expected graduation date between&nbsp;May 2028 –&nbsp;Dec&nbsp;2028&nbsp;</p><br></li></ul><ul><li><p>Must be able to commit to a 6-month duration in-person at AbbVie Bioresearch Center (ABC) in Worcester, MA (July - December).&nbsp;</p><br></li></ul><p><strong>Preferred Qualifications&nbsp;</strong></p><br><ul><li><p>Strong communication, adaptability, networking, and creative problem-solving skills&nbsp;</p><br></li></ul><ul><li><p>Exposure to computerized maintenance management and business systems, including Maximo, SAP, and SharePoint&nbsp;</p><br></li></ul><br>Additional Information<br><br><p><strong>Benefits and Amenities:</strong><br>Competitive pay<br>Relocation support for eligible students<br>Select wellness benefits and paid holiday / sick time<br><strong>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​</strong><br>​The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​<br>​<br>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision spending 6 months working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie AbbVie Co-Ops. </p><br><p>AbbVie PDST Analytical Development supports biologics development through analytical characterization, method development, and scientific investigation of product quality attributes. The team collaborates across functions to generate data and insights that enable process development, product understanding, and regulatory readiness. Co-ops contribute to analytical studies, data analysis, and technology development while gaining hands-on experience in a fast-paced biopharmaceutical development environment. </p><br><p><strong>Key responsibilities include: </strong></p><br><ul><li><p>Supporting the development and evaluation of analytical methods for biologics characterization, with a focus on chromatographic and mass spectrometry-based techniques.&nbsp;</p><br></li></ul><ul><li><p>Performing laboratory experiments, including sample preparation, instrument operation, and data collection, under appropriate guidance.&nbsp;</p><br></li></ul><ul><li><p>Analyzing and interpreting experimental data to identify trends, differences across process conditions, and potential product quality attributes.&nbsp;</p><br></li></ul><ul><li><p>Supporting characterization of ADCs, or other complex biologic molecules using techniques such as LC-MS, and related analytical platforms.&nbsp;</p><br></li></ul><ul><li><p>Assisting with the development of efficient analytical screening workflows to support process development and sample comparison.&nbsp;</p><br></li></ul><ul><li><p>Organizing, visualizing, and summarizing analytical results for technical discussions, presentations, and project updates.&nbsp;</p><br></li></ul><ul><li><p>Collaborating with analytical, process development, and other cross-functional teams to support project objectives.&nbsp;</p><br></li></ul><ul><li><p>Maintaining accurate experimental records and follow established laboratory procedures and safety requirements.</p><br></li></ul><br>Qualifications<br><br><p><strong>Minimum Qualifications </strong></p><br><ul><li><p>Currently enrolled in a university and pursuing a Master’s degree in analytical chemistry, biochemistry, chemistry, pharmaceutical sciences, chemical engineering, or a related field.&nbsp;</p><br></li></ul><ul><li><p>Must be enrolled in university for at least one semester following the co-op.&nbsp;</p><br></li></ul><ul><li><p>Expected graduation date between May 2028 – Dec 2028.&nbsp;</p><br></li></ul><ul><li><p>Strong written and verbal communication skills.&nbsp;</p><br></li></ul><ul><li><p>Ability to work both independently and collaboratively in a laboratory and cross-functional team environment.&nbsp;</p><br></li></ul><ul><li><p>Willingness to learn new analytical techniques and follow established laboratory safety and documentation practices.&nbsp;</p><br></li></ul><ul><li><p>Must be able to commit to a 6-month program at AbbVie’s site located in Waltham, MA (July - December). </p><br></li></ul><p><strong>Preferred Qualifications&nbsp;</strong></p><br><ul><li><p>Exposure to liquid chromatography, mass spectrometry, or protein characterization </p><br></li></ul><ul><li><p>Research experience in analytical chemistry, protein science, or biologics&nbsp;</p><br></li></ul><br>Additional Information<br><br><p><strong>Benefits and Amenities:</strong></p><br><ul><li>Competitive pay</li><li>Relocation support for eligible students</li><li>Select wellness benefits and paid holiday / sick time</li></ul><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the&nbsp;time&nbsp;of&nbsp;this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic&nbsp;location,&nbsp;and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The&nbsp;amount&nbsp;and&nbsp;availability&nbsp;of any&nbsp;bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's&nbsp;sole&nbsp;and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>The Principal Scientist I will be an integral part of the Process Analytics team in the Operations – Product Development Science and Technology – Biologics division. The role involves leading analytical activities within a high-throughput testing group supporting biologics products with a focus on advancing AbbVie’s late-stage clinical programs. This position calls for an individual with a strong technical analytical background, demonstrated leadership and organizational skills and the ability to effectively communicate and work cross-functionally.</p><br><p><strong>Responsibilities:</strong></p><br><ul><li>Lead analytical activities within a high-throughput testing group supporting biologics process development for late-stage programs.</li><li>Serve as the subject matter expert for separation-based methods, including HPLC and capillary electrophoresis.</li><li>Evaluate and select effective fit for purpose analytical technologies and methods to meet process development needs.</li><li>Provide expertise and support for method development, execution, and troubleshooting. Provide direct technical guidance and oversight to scientists executing sample testing with hands on lab support when needed.</li><li>Partner with process development SMEs for interpretation and understanding of analytical data.</li><li>Oversee sample testing schedule and prioritization; drive timely delivery of high-quality testing results.</li><li>Support implementation of automation and high-throughput experimentation workflows.</li><li>Drive continuous improvement initiatives to enhance lab efficiency and capability.</li><li>Mentor, train and supervise junior scientists.</li></ul><br>Qualifications<br><br><ul><li>PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline with 6+ years of relevant professional experience working in analytical development or process analytics; MS degree with minimum of 10+ years of relevant experience.</li><li>Proven experience leading analytical development activities for biologics development, including mAbs, multi-specifics, antibody-drug conjugates, and fusion proteins.</li><li>Hands on method development experience in protein and impurity analysis techniques such as HPLC, capillary electrophoresis, and other relevant methods for biologics required. Experience with mass spectrometry and ELISA is a plus.</li><li>Previous experience with automation is a plus.</li><li>Highly organized with ability to multitask and drive efficient workflows.</li><li>Ability to think critically and demonstrate troubleshooting and problem-solving skills.</li><li>Strong people leadership skills and demonstrated ability to foster an engaging, inclusive and collaborative team environment. Direct people management experience required.</li><li>Excellent communication and interpersonal skills. Ability to work effectively across functions, anticipating and addressing overall program development needs.</li><li>An independent, self-motivated, proactive individual who thrives in a fast-paced team environment.</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li><li>This job is eligible to&nbsp;participate&nbsp;in our long-term incentive&nbsp;programs.&nbsp;</li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>The Principal Research Scientist I will be an integral part of the Late-Stage Process Analytics group within the Analytical Development team in the Operations – Product Development Science and Technology – Biologics division. The role involves supporting analytical aspects of biologics products with a focus on advancing AbbVie’s late-stage clinical programs. This position calls for an individual with a strong technical analytical background, demonstrated leadership skills and the ability to effectively communicate and work cross-functionally. </p><br><p>Responsibilities:&nbsp;</p><br><ul><li>Serve as the process analytics lead for mab and DS in AbbVie's CMC teams, supporting late-stage biologics pipeline assets. Act as a partner to the process development groups. Balance stakeholder expectations to ensure effective collaboration. </li><li>Serve as the subject matter expert for separation-based methods including HPLC and capillary electrophoresis for sample testing to support biologics mab and DS process development, characterization, validation as well as GMP manufacturing investigation activities.&nbsp;</li><li>Evaluate and select effective analytical technologies and methods to meet program needs. </li><li>Support timely delivery of high-quality testing results. </li><li>Provide expertise and support for method development, execution, and troubleshooting.&nbsp;</li><li>Provide hands-on support in the lab as needed. </li><li>Review analytical results; communicate analytical issues and risks to relevant teams. Promote proactive risk resolution within and across functional areas to advance project objectives.&nbsp;</li><li>Collaborate with other analytical teams in R&amp;D and PDS&amp;T on program transition, workflow and alignment. </li><li>Participate in the preparation and review of technical documents for late-stage programs. Author and review analytical sections of IND/BLA filings. </li><li>Demonstrate scientific excellence, advance science and innovation. Implement novel analytical techniques to enhance method robustness and expand analytical capabilities. </li><li>Mentor and/or supervise junior scientists.&nbsp;</li></ul><br>Qualifications<br><br><ul><li>PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline. Minimum of 6+ years (PhD) of relevant professional experience working in biotech/pharmaceutical setting.&nbsp;</li><li>Proven experience with analytical activities supporting biologics development, including mAbs, multi-specifics, antibody-drug conjugates, and fusion proteins. Late-stage program experience preferred.&nbsp;</li><li>Expertise in protein and impurity analysis techniques such as HPLC, capillary electrophoresis, and other relevant methods. </li><li>Skilled in technical writing including experience in authoring, reviewing regulatory submissions and responding to agency information requests. </li><li>Strong leadership skills and demonstrated ability to foster an engaging, inclusive and collaborative team environment.&nbsp;</li><li>Excellent communication and interpersonal skills, effectively managing relationships to enhance team decision-making.&nbsp;</li><li>Ability to work effectively across functions, anticipating and addressing overall program development needs. </li><li>Ability to quickly comprehend and adapt to new situations, with an open mindset and can-do attitude, demonstrating agility where necessary to address evolving project needs. </li><li>Ability to think critically and demonstrate troubleshooting and problem-solving skills. High attention to detail. </li><li>Ability to lead and manage multiple projects of significant scope and complexity, while meeting all deliverables and timelines. </li><li>An independent, self-motivated, proactive individual who thrives in a fast-paced team environment.&nbsp;</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li><p>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</p><br></li><li><p>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</p><br></li><li><p>This job is eligible to&nbsp;participate&nbsp;in our long-term incentive&nbsp;programs.&nbsp;​</p><br></li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Conceive and implement novel experimental approaches to answer scientific questions. Investigate, identify, develop, and optimize new methods and techniques. Contribute to project science in area of expertise. Develop productive collaborations and communications with other groups across science disciplines.</p><br><p>Responsibilities:&nbsp;</p><br><ul><li>Develop robust downstream processes for early-stage and late-stage pipeline molecules to support CMC activities for various programs and improve tech transfer workflows. Drive commercial process development for purification within project timelines</li><li>Drive continuous improvement initiatives and next-generation platform development, including identification and modeling of COGs, process fits, and intensification gains</li><li>Optimize downstream purification unit operations using experimentation and modeling approaches and identifying avenues for process characterization acceleration</li><li>Design and execute process development and characterization activities. Highly independent and productive in performing laboratory experimentation.</li><li>Play a key role in deeply understanding downstream unit operations to build a deep scientific understanding of existing platform processes and impact on manufacturability</li><li>Exhibit a strong motivation to implement and advance various innovative technologies in relevant areas across AbbVie (such as AI, automation, and digital transformation)</li><li>Routinely demonstrate scientific initiative and creativity in research/development activities. Act as primary author of publications, presentations, regulatory documents, and/or become the primary inventor of patents</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled substances, and GxP compliance</li></ul><br>Qualifications<br><br><ul><li>BS or MS in Biological science with focus in Immunology, Biochemistry, Molecular Biology, Cell Biology, or a related discipline with typically 7+ (BS) or 5+ (MS) years of relevant lab experience.</li><li>Possess thorough theoretical and practical understanding of own scientific discipline.</li><li>Education background in chemical engineering, biochemistry, biochemical engineering, or biotechnology is preferred.</li><li>Experience in downstream process intensification or modeling is preferred</li><li>Experience in areas of purification process development is strongly preferred.</li><li>Demonstrate excellent communication skills and specifically illustrate strong oral and written technical communications.</li><li>Seamlessly present research outcomes to multifunctional teams</li><li>Play a strong team player in a cross functional collaborative environment thriving for world class excellence and maintains strong working relationships with internal, global, and external collaborators.</li><li>Demonstrated problem-solving skills and capability to overcome complex issues.</li><li>Demonstrated success in coordinating and executing important projects to achieve business goals.</li><li>Must have a “results-oriented” work ethic and a positive “can-do” attitude with a strong sense of urgency and self-motivated desire to achieve.</li></ul><br>Additional Information<br><br><p>​Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the&nbsp;time&nbsp;of&nbsp;this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic&nbsp;location,&nbsp;and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li><li>This job is eligible to&nbsp;participate&nbsp;in our short-term incentive&nbsp;programs.&nbsp;​</li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The&nbsp;amount&nbsp;and&nbsp;availability&nbsp;of any&nbsp;bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's&nbsp;sole&nbsp;and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p><strong>Purpose</strong></p><br><p>The Global Process Support Engineer (Aseptic) will support the AbbVie Technical Operations Functions and the AbbVie Technical Centers worldwide. This position will be responsible for applying advanced scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete complex assignments related to aseptic capital projects and aseptic process troubleshooting. The selected candidate will contribute to the development of new principles and concepts and is expected to lead change from an engineering perspective. Will also be responsible for solving operating issues and providing technical support to cross-functional teams within the Aseptic sites.</p><br><p><strong>Responsibilities</strong></p><br><ul><li>Serves as organization spokesperson on advanced projects and/or programs related to aseptic operation including equipment selection. Presents results of projects both internally and externally.</li><li>Acts as advisor to management and operating sites on applications of new advanced processing equipment and participates in project planning, process update</li><li>Responsible for timely project completion.</li><li>May act as lead engineer, project leader, or project contributor.</li><li>Ensures quality and effectiveness of aseptic solutions as part of major projects through sound design, early risk assessments, and implementation strategies. Has full awareness of the potential consequences (defects and failure modes) of design changes to established processes.</li><li>Evaluates and integrate relevant engineering advances for improving or solving problems.</li><li>Understands the business implications of assigned products and processes and identify engineering solutions compatible with business needs.</li><li>Provides technical direction and feedback to others.</li><li>Responsible for compliance with applicable corporate and local policies and procedures.</li></ul><p>#LI-AL1</p><br><br>Qualifications<br><br><p>MS or PHD in Mechanical, Chemical Engineering or related field with 6 to 8 years of engineering experience in pharmaceutical aseptic process design, equipment selection and operation in one of the following areas:</p><br><p>• general aseptic processing;</p><br><p>• upstream and downstream biological processing;</p><br><p>• aseptic fill finishing</p><br><p>Good knowledge of:</p><br><p>• Aseptic fill finish technology and suppliers</p><br><p>• Broader compounding, built infrastructure (cleanroom design, services (water, HVAC…..)</p><br><p>• Knowledge of regulatory environment and requirements both in Europe and the US</p><br><p>• Methods of Microbial control and environmental monitoring</p><br><p>• Control and information systems used in secondary pharma and fill finish on particular</p><br><p>• Understands both equipment control and SCADA and MES levels.</p><br><p>• Secondary packaging</p><br><p>• Single use systems</p><br><p>• Cleaning and sanitisation methodologies.</p><br><p>• Knowledge about associated technology (Lyophilisation, Blow Fill Seal)</p><br><p>• Application of robotics</p><br><p>Understanding of:</p><br><p>• typical process analysis and troubleshooting tools.</p><br><p>• high containment processing</p><br><p>• change control requirements</p><br><p>• key literature beyond regulations (ISPE, AMSE, ISO, USP)</p><br><p>• project costing, lead times, control and management</p><br><p>• broader commercial environment in the Pharma industry.</p><br><p>Experience:</p><br><p>• Demonstrated excellence in breadth and depth of knowledge within the aseptic discipline and is recognized as a subject matter expert</p><br><p>• Experience active participating or leading FMEA, Risk Assessments and/or Investigations for aseptic pharmaceutical processes.</p><br><p>• Must demonstrate negotiation skills and ability to reconcile differences</p><br><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li><p>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of thisposting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location,and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</p><br></li><li><p>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</p><br></li><li><p>This job is eligible to&nbsp;participate&nbsp;in our long-term incentive&nbsp;programs.&nbsp;​</p><br></li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission,incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's sole and&nbsp;absolute&nbsp;discretion unless anduntil paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> Company culture : <p><strong>Manpower Agences</strong> operates within a highly balanced culture, where <strong>collaboration</strong> plays a key role in the work environment. The company values close leadership, trust and collective engagement, while placing equal importance on <strong>performance</strong> and achieving results. This dynamic is supported by a <strong>structured organizational approach</strong>, promoting rigor, efficiency and quality execution. Openness to innovation further strengthens this balance, supporting adaptability in an evolving market. </p><br><br> <br> Job : <p>Responsible for environmental, health, and safety (EHS) management within a large-scale industrial manufacturing environment. Establish and continuously improve an EHS management system that complies with Moroccan regulations and international standards. Ensure regulatory compliance, employee safety, and environmental performance during both construction and operational phases, while promoting best practices in sustainable and safe manufacturing.</p><br><br><p><u><strong>Key Responsibilities :</strong></u><br><strong>1. EHS System Development and Strategic Planning</strong></p><br><br><ul><li>Establish and continuously improve the EHS management system in accordance with ISO 14001, ISO 45001, ISO 50001, and applicable Moroccan regulatory requirements.</li><li>Develop annual EHS objectives, performance indicators, and implementation plans.</li><li>Integrate EHS requirements into all operational and production processes and drive continuous improvement initiatives.</li><li>Implement EHS policies, audit requirements, and reporting mechanisms to ensure effective governance and performance monitoring.</li></ul><p><strong>2. Regulatory Compliance and Government Liaison</strong></p><br><br><ul><li>Monitor and ensure compliance with Moroccan labor, environmental, health, and safety legislation.</li><li>Coordinate communications and inspections with labor authorities, environmental agencies, fire departments, and other regulatory bodies.</li><li>Ensure all required permits, authorizations, environmental approvals, and certifications remain valid and up to date.</li><li>Conduct compliance assessments against applicable environmental regulations and lead corrective action plans when required.</li><li>Coordinate government inspections, external audits, and stakeholder inquiries related to EHS matters.</li></ul><p><strong>3. Occupational Health and Safety Management</strong></p><br><br><ul><li>Conduct hazard identification and risk assessments covering chemicals, machinery, electrical installations, work at height, and confined spaces.</li><li>Implement and monitor risk mitigation and control measures.</li><li>Oversee EHS performance of contractors, subcontractors, and construction companies, including qualification reviews and approval of work and emergency response plans.</li><li>Lead investigations of workplace incidents, injuries, and near misses, and ensure implementation of corrective and preventive actions.</li><li>Manage fire protection systems and emergency response capabilities, including drills and preparedness exercises.</li><li>Coordinate occupational health programs, industrial hygiene monitoring, and employee medical surveillance activities.</li><li>Develop and deliver EHS training programs, including induction training, technical safety training, and leadership awareness initiatives.</li></ul><p><strong>4. Environmental Management and Sustainability</strong></p><br><br><ul><li>Ensure compliant management, storage, treatment, and disposal of waste, hazardous materials, wastewater, emissions, and chemicals.</li><li>Maintain traceability systems and environmental records.</li><li>Monitor environmental risks associated with industrial operations, including chemical handling, emissions control, and environmental protection measures.</li><li>Track energy consumption and carbon footprint indicators and support sustainability and ESG-related initiatives.</li><li>Promote energy efficiency, resource conservation, and emissions reduction programs.</li><li>Support biodiversity protection initiatives and maintain positive environmental relationships with surrounding communities.</li></ul><p><strong>5. Stakeholder Management and Supply Chain EHS Control</strong></p><br><br><ul><li>Maintain effective communication with local communities, authorities, regulatory bodies, and industry stakeholders regarding EHS matters.</li><li>Conduct EHS assessments and audits of suppliers, contractors, logistics providers, and waste management companies.</li><li>Develop contractor and supplier EHS performance evaluation processes.</li><li>Integrate EHS requirements into supplier qualification, onboarding, and performance review processes.</li><li>6. Team Development and Safety Culture</li><li>Build and develop a high-performing EHS team through clear role definition, competency development, and succession planning.</li><li>Promote a strong safety culture through behavioral safety programs, safety observations, awareness campaigns, and employee engagement initiatives.</li><li>Encourage workforce participation in EHS improvement programs and initiatives.</li><li>Prepare regular EHS performance reports for leadership and provide recommendations for continuous improvement.</li></ul> <br> <br> Required profile : <p><u><strong>Qualifications :</strong></u></p><br><br><p><strong>1. Education</strong></p><br><br><ul><li>Bachelor's degree or higher in Safety Engineering, Environmental Engineering, Occupational Health, Chemical Engineering, or a related field.</li></ul><p><strong>2. Work Experience</strong></p><br><br><ul><li>Minimum 5 years of experience in EHS management within an industrial or manufacturing environment, including at least 2 years in a managerial or supervisory EHS role.</li><li>Experience in sectors such as manufacturing, chemicals, energy, infrastructure, heavy industry, or large-scale construction projects is highly desirable.</li><li>Experience within multinational or international industrial organizations is considered an advantage.</li></ul><p><strong>3. Professional Competencies</strong></p><br><br><ul><li>Strong knowledge of ISO 14001 and ISO 45001 management systems, including implementation, continuous improvement, internal audits, and external audit coordination.</li><li>Solid understanding of Moroccan labor, environmental, health, and safety regulations, with experience managing compliance requirements and interactions with regulatory authorities.</li><li>NEBOSH, IOSH, or other recognized international EHS certifications are preferred.</li><li>Proven expertise in chemical safety management, fire prevention and protection systems, emergency preparedness, and incident response.</li></ul><p><strong>4. Language Skills</strong></p><br><br><ul><li>Fluency in Arabic and/or French, with the ability to manage professional communications, regulatory documentation, and interactions with local authorities.</li><li>Good command of English, both written and spoken, allowing effective communication within an international business environment.</li></ul><p><strong>5. Other Competencies</strong></p><br><br><ul><li>Strong cross-cultural communication and stakeholder management skills.</li><li>Excellent organizational, coordination, and problem-solving abilities.</li><li>Sound risk assessment and decision-making capabilities in complex and dynamic operational environments.</li><li>Ability to manage multiple priorities simultaneously and support activities during both project and operational phases.</li></ul> <br><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>Envision working with energetic colleagues and inspirational leaders, all while gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie’s Co-Ops. This is a work experience and is not intended to support a thesis. </p><br><p>Product Development Science and Technology (PDS&amp;T): Designs, delivers, and supports biologics manufacturing processes for AbbVie’s pipeline and partnered products through clinical development and commercial life cycle. The department advances targeted product quality, CMC acceleration, people development, and efficient workflows, bringing together expertise across Cell Line Development, Cell Culture Process Development, Purification Process Development, Scale-Up Lab, and Analytical Development.&nbsp;</p><br><p>We are seeking an exceptional graduate co-op student to join our Cell Culture Development and Automation team for an innovative, hands-on project at the intersection of optical spectroscopy, cell culture science, laboratory robotics, and data analytics. In this role, you will help integrate spectroscopy with automated liquid-handling robotics to enable rapid, at-line characterization of cell-culture product quality and metabolites. You will have the opportunity to build novel hardware, develop automated analytical workflows, and apply chemometric and data-science modeling to production-relevant datasets, helping transform how process development teams learn from experiments.&nbsp;</p><br><p><strong>Key responsibilities include:&nbsp;</strong></p><br><ul><li><p>Supporting integration of spectroscopy systems with an automated liquid-handling platform for high-throughput, at-line spectral acquisition from cell culture samples.&nbsp;</p><br></li></ul><ul><li><p>Designing and 3D printing custom labware and sampling components to support automated sample transfer and spectral measurement.&nbsp;</p><br></li></ul><ul><li><p>Developing and troubleshoot automated liquid-handler methods for sample acquisition, flow-cell delivery, and system wash and cleaning cycles.&nbsp;</p><br></li></ul><ul><li><p>Performing aseptic cell culture techniques, including thawing, passaging, and banking of mammalian (CHO) cell lines, to support experimental studies.&nbsp;</p><br></li></ul><ul><li><p>Collecting, processing, and analyzing Raman spectral and process data; apply chemometric and data-science techniques to build predictive models for metabolites and product quality attributes.&nbsp;</p><br></li></ul><ul><li><p>Collaborating cross-functionally with scientists in cell culture development, automation engineering, and analytical development to refine workflows using experimental results and team feedback.&nbsp;</p><br></li></ul><ul><li><p>Documenting experimental methods, data, and results clearly; contribute to a final presentation and/or manuscript-quality summary suitable for internal or external scientific communication.&nbsp;</p><br></li></ul><br>Qualifications<br><br><p><strong>Minimum Qualifications </strong></p><br><ul><li><p>Currently enrolled in university, pursuing a Master’s degree in Chemical Engineering, Biochemical Engineering, Bioengineering, Chemistry or a related field.&nbsp;</p><br></li></ul><ul><li><p>Must be enrolled in university at the time of the Co-Op.&nbsp;</p><br></li></ul><ul><li><p>Expected graduation date between May 2028 – Dec 2028&nbsp;</p><br></li></ul><ul><li><p>Proficient in aseptic techniques, including thawing, passaging, and banking mammalian cell lines in a biosafety cabinet.&nbsp;</p><br></li></ul><ul><li><p>Knowledge of optical spectroscopy techniques, including Raman, fluorescence, and absorbance.&nbsp;</p><br></li></ul><ul><li><p>Knowledge of biology and biochemistry, cell metabolism, and protein characterization as applied to CHO cell culture development.&nbsp;</p><br></li></ul><ul><li><p>Must be able to commit to a 6-month program at AbbVie’s site located in Worcester, MA (June&nbsp;- December). </p><br></li></ul><p><strong>Preferred Qualifications&nbsp;</strong></p><br><ul><li><p>Strong critical-thinking skills and the ability to troubleshoot complex laboratory robotics and instrumentation challenges.&nbsp;</p><br></li></ul><ul><li><p>Ability to design and create custom labware using 3D printing.&nbsp;</p><br></li></ul><ul><li><p>Ability to execute, troubleshoot, and interpret complex experimental data to determine thoughtful next steps.&nbsp;</p><br></li></ul><ul><li><p>Working knowledge of programming or scripting languages such as Python, Visual Basic and C/C++.&nbsp;</p><br></li></ul><br>Additional Information<br><br><p><strong>Benefits and Amenities:</strong></p><br><ul><li>Competitive pay</li><li>Relocation support for eligible students</li><li>Select wellness benefits and paid holiday / sick time</li></ul><p>​Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the&nbsp;time&nbsp;of&nbsp;this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic&nbsp;location,&nbsp;and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;</li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The&nbsp;amount&nbsp;and&nbsp;availability&nbsp;of any&nbsp;bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's&nbsp;sole&nbsp;and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>AbbVie is searching for a highly motivated individual to fill a Senior Scientist I/ position in the Analytical Development Department at AbbVie Bioresearch Center in Worcester MA. The Analytical Development Department is responsible for development, qualification and execution of analytical methods and characterization studies to provide product and process understanding for development of AbbVie biopharmaceutical pipeline from discovery through commercial stages.</p><br><p>Analytical Development is seeking a highly experienced, motivated and team-oriented individual for an important role supporting development of AbbVie’s biologic pipeline of preclinical and clinical products. The successful candidate will be a member of the Process Analytics team responsible for development and execution of various separation methods (HPLC, CE, icIEF, etc.) and other analytical methods (small scale purification, SoloVPE, etc.) to support the CMC development of AbbVie early phase products and processes throughout the drug development lifecycle.&nbsp;</p><br><p>Key Responsibilities:</p><br><ul><li>Independently develop and apply capillary electrophoresis, and HPLC methods separation as well as other analytical methods to enable biological process development</li><li>Develop, qualify, and transfer fit-for-purpose in-process control methods to QC.&nbsp;</li><li>Provide technical support to QC testing occurring at internal and external GMP testing laboratories.</li><li>Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.</li><li>Publish research in peer-reviewed journals and present work at scientific conferences.</li><li>Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program.</li><li>Seize opportunities to pursue project relevant leads that are in line with the group’s strategy.</li><li>Maintain a high level of productivity in the lab.</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.</li><li>May mentor/supervise a team of one or more and guide and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.</li><li>Represent analytical function in the CMC program team; represent the Analytical Development Group as a subject matter expert on cross functional teams. Lead the development of analytical control strategy for biologic programs&nbsp;</li><li>Plan and author internal technical reports as well as relevant CMC sections of regulatory submissions (INDs/CTDs).</li><li>Identify and lead analytical innovations to further scientific capability of the group.</li></ul><br>Qualifications<br><br><ul><li>PhD Degree and 0-4+ years or MS with 10+ years of experience within Biochemistry, Chemical Engineering, Analytical Chemistry, Pharmaceutical Science (or related discipline) in industry or academia. </li><li>Possess thorough theoretical and practical understanding of own scientific discipline.</li><li>Effective writer and communicator of research or other regulatory materials.</li><li>Must have strong written and verbal communications skills.</li></ul><p>Preferred Qualifications:</p><br><ul><li>Ability to work effectively cross-functionally in anticipating and responding to overall program development needs</li><li>Demonstrated record of independent thought, creativity and scientific accomplishment&nbsp;</li><li>Self-motivated with the ability to act with urgency and passion</li><li>Ability to make thoughtful, integrated, timely and meaningful recommendations and/or decision and take corresponding actions</li><li>Experience with CMC analytical development of monoclonal antibodies or related biotherapeutic proteins is a plus.</li></ul><p>Key Leadership Competencies:</p><br><ul><li>Delivers business results while also positioning AbbVie for long-term success</li><li>Raises the bar and is never satisfied with the status quo</li><li>Creates a learning environment, open to suggestions and experimentation for improvement</li><li>Embraces the ideas of others, nurtures innovation and manages innovation to reality</li></ul><br>Additional Information<br><br><p><br>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li><li>This job is eligible to&nbsp;participate&nbsp;in our long-term incentive&nbsp;programs.&nbsp;</li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p>The Senior Scientist I will be part of a centralized modeling team supporting the development and implementation of a broad range of models across early- and late-stage bioprocess development for diverse biologic modalities, including monoclonal antibodies, antibody-drug conjugates, bispecifics, and gene therapies. Working collaboratively across functions, the scientist will develop and apply innovative modeling and experimental approaches to address scientific and process development challenges, including scale-up and technology transfer. The team’s mission is to continually build next-generation modeling capabilities through deep integration with artificial intelligence (AI) tools, delivering business impact with agility.</p><br><p>Responsibilities:&nbsp;</p><br><ul><li>Independently conceptualize, build, and apply fit-for-purpose models for upstream cell culture and downstream purification processes across early- and late-stage bioprocess development.</li><li>Translate scientific and business challenges into modeling strategies that deepen process understanding, guide process optimization, and support scale-up and technology transfer.</li><li>Advance next-generation modeling capabilities through deep integration with AI tools to accelerate model development and implementation and deliver business impact with agility.</li><li>Work closely with the Automation and Digitalization team to establish data workflows and integrated tools that enable efficient model building and implementation.</li><li>Integrate multidisciplinary data and scientific fundamentals to assess model performance, assumptions, and limitations, draw actionable conclusions, and resolve key project challenges.</li><li>Collaborate in an agile, fast-paced matrix team spanning IT, Data Science, CMC, and Development to align priorities, adapt to evolving needs, and deliver modeling solutions; provide scientific mentorship and technical guidance as appropriate.</li><li>Communicate modeling approaches, results, limitations, and recommendations clearly and efficiently to project teams and leadership to support timely, informed decisions.</li><li>Support model transfer and lifecycle management, including implementation, documentation, maintenance, updates, and assessment of continued fitness for purpose, in accordance with applicable corporate, safety, and GxP standards.</li><li>Serve as a primary author of modeling-related technical and regulatory documents, peer-reviewed publications, and scientific presentations, and contribute to patentable innovations as appropriate.</li><li>Proactively evaluate relevant literature and emerging technologies, identify innovative modeling opportunities aligned with the centralized team’s strategy, and incorporate advances into projects and broader modeling capabilities.</li></ul><br>Qualifications<br><br><ul><li>Bachelor’s degree or equivalent education and typically 10 years of experience, Master’s degree or equivalent education and typically 8 years of experience, PhD degree or equivalent education and 0-2 years of experience.</li><li>Education background in chemical engineering, biomedical engineering, biochemistry, biochemical engineering, or biotechnology is preferred.</li><li>Experience in both upstream cell culture and downstream purification process development is preferred. Demonstrated expertise in computational fluid dynamics (CFD) modeling, cell culture kinetics and metabolic flux balance modeling, chromatography modeling, and filtration theory and modeling is preferred.</li><li>Familiarity with AI tool development and experience integrating AI tools into the bioprocess development ecosystem.</li><li>Demonstrate excellent communication skills and specifically illustrate strong oral and written technical communications. Seamlessly present research outcomes to multifunctional teams</li><li>Play a strong team player in a cross functional collaborative environment thriving for world class excellence and maintains strong working relationships with internal, global, and external collaborators.</li><li>Demonstrated problem-solving skills and capability to overcome complex issues.</li><li>Demonstrated success in coordinating and executing important projects to achieve business goals.</li><li>Must have a “results-oriented” work ethic and a positive “can-do” attitude with a strong sense of urgency and self-motivated desire to achieve.</li></ul><br>Additional Information<br><br><p>Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​</p><br><ul><li>The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the&nbsp;time&nbsp;of&nbsp;this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic&nbsp;location,&nbsp;and&nbsp;we&nbsp;may&nbsp;ultimately&nbsp;pay&nbsp;more or less than the posted range. This range may be&nbsp;modified&nbsp;in the&nbsp;future.&nbsp;​</li><li>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​</li><li>This job is eligible to&nbsp;participate&nbsp;in our short-term incentive&nbsp;programs.&nbsp;​</li></ul><p>Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The&nbsp;amount&nbsp;and&nbsp;availability&nbsp;of any&nbsp;bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee&nbsp;remains&nbsp;in the Company's&nbsp;sole&nbsp;and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be&nbsp;modified&nbsp;at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;​</p><br><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div>