Quality Control Analyst (CDD - 1 year contract) page is loaded

Quality Control Analyst (CDD - 1 year contract)

Quality Control Analyst (CDD - 1 year contract)

locationsMorocco - El Jadida time typeVoltijds posted onVandaag geplaatst job requisition id4926807 Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. Your knowledge of quality control will be helpful to support our quality programs. Your ability to analyze chemical, biological or microbiological products will help us manage our quality. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to its patients.
Your qualifications of unique Quality Control instruments will help us meet accuracy specifications for sample management, retains managements, interpretation and evaluation.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

Perform analytical testing accurately and efficiently and in accordance to Standard Operating Procedures (SOPs).
Perform equipment verification and calibration in accordance to procedures.
Document all results in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.
Ensure all quality records are attached and/or file as predetermined.
Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements and that they are filed in accordance to existing policies.
Participate actively and contribute to site project teams.
Advise on the significance of test results and follow up with appropriate course of actions.
Actively participate in Safety initiatives, typically a role model for other analyst. Ability to perform investigation related to EHS.
Participate in 5S team initiatives and practice good housekeeping.
Participate in laboratory investigations/incidents such as out of specification investigation and equipment troubleshooting investigations, identify root causes and implement appropriate corrective action and preventive measures.
Commitment to work and positive influencer/role model/motivate others for overall operational excellence.

Job Related Requirements:

Demonstrated leadership and customer service skills. Effective problem solving skills. Strong verbal, written communication, and presentation skills. Demonstrated ability to perform in a team. Comprehensive knowledge of cGMPs and appropriate regulations. Comprehensive knowledge of HPLC, GC and laboratory equipment. Experience in Empower software will be an added advantage.

Accountability:

Analytical testing
Laboratory Non-conformance and Investigation management. Laboratory safety and housekeeping Procedures Development & Review Training

Qualifications

Must-Have
Bachelor's degree in science with 1 year experience in related field Demonstrated technical skills in chemical and physical testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures. Knowledge of Good Manufacturing Practices and its application standards, processes and policies Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills

Nice-to-Have

Laboratory work experience with analytical HPLC (High Pressure Liquid Chromatography) technique Experience leading continuous improvement projects
Position Based in El Jadida, Morocco
CDD - 1 year contract
End date posted: 8th January, 2025
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control#LI-PFE