Quality Control Analyst (CDD - 6 mois)

Use Your Power for Purpose

Everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. You will play a crucial role in improving patients' lives by ensuring the highest standards of Good Manufacturing Practices (GMP) are met. Your work will directly contribute to the safety and efficacy of our products, making a tangible difference in the lives of patients worldwide.

What You Will Achieve

In this role, you will:

• Perform analytical and/or microbial testing accurately and efficiently following Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.

• Interpret and evaluate data in terms of accuracy, precision and potential good manufacturing Practices impact and recommend appropriate corrective actions.
• Support the troubleshooting and resolution of equipment and testing issues, ensuring operational readiness.
• Manage and maintain reagents, references standards and laboratory consumables inventories, ensuring they are valid and stored correctly.
• Support routine data review following written procedures.
• Maintain training to current standards and procedures on all assigned curriculums
• Participate in Laboratory investigations and propose CAPA for the identified root cause.
• Contribute to the completion of improvement projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.

• Manage personal time and professional development, being accountable for results.

• Maintain data integrity and ensure compliance with company SOPs, GLP and cGMP regulations.

• Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures for site and QC laboratories are followed.

Here Is What You Need (Minimum Requirements):

• Bachelor's degree (Chemistry, Biology, Biotechnology or similar)

• First experience in the pharmaceutical industry is highly appreciated

• Knowledge of laboratory equipment, testing, and techniques
• Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
• Excellent organizational skills and strong ability to multi-task across various projects and activities
• Strong written and verbal communication skills (French and English)
• High level of attention to detail
• Self-motivated and able to work in minimal direction
• Broad experience with Microsoft Office products

Bonus Points If You Have (Preferred Requirements):

• Ability to manage multiple priorities and meet deadlines.
• Ability to work independently and as part of a team
• Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
• Adaptability and willingness to learn new techniques and procedures

• Experience using common AI tools, including generative technologies such as Microsoft Copilot, to support problem solving and enhance productivity.

Work Location Assignment: On Site

Worker Type: CDD 6 months

  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.


Quality Assurance and Control