Quality Control Analyst (CDD - 1 year contract)

Posted 15 Hours Ago
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El Jadida
Hybrid
Entry level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
As a Quality Control Analyst, you will ensure the delivery of safe and effective products by performing analytical testing, equipment verification, and documentation in line with GMP and GLP. You will participate in team initiatives related to laboratory safety and operational excellence, contributing to quality assurance and control efforts.
Summary Generated by Built In

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

Top Skills

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What the Team is Saying

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The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Employees engage in a combination of remote and on-site work.

Typical time on-site: Not Specified
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