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We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Perform GMP/GLP-compliant analytical and microbial testing, review and interpret data, support troubleshooting and investigations, maintain lab inventories and training, propose CAPAs, ensure data integrity and SOP compliance, and contribute to continuous improvement and 5S initiatives.
Summary Generated by Built In
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:
Here Is What You Need (Minimum Requirements):
Bonus Points If You Have (Preferred Requirements):
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
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
Skills Required
- Bachelor's degree (Chemistry, Biology, Biotechnology or similar)
- First experience in the pharmaceutical industry
- Knowledge of laboratory equipment, testing, and techniques
- Knowledge of Good Manufacturing Practices (GMP) and its application standards, processes, and policies
- Excellent organizational skills and ability to multi-task
- Strong written and verbal communication skills (French and English)
- High level of attention to detail
- Self-motivated and able to work with minimal direction
- Broad experience with Microsoft Office products
- Ability to manage multiple priorities and meet deadlines
- Ability to work independently and as part of a team
- Excellent interpersonal skills and ability to communicate effectively
- Adaptability and willingness to learn new techniques and procedures
- Experience using common AI tools, including generative technologies such as Microsoft Copilot
What the Team is Saying
Daniel
Diagnostics Launch Lead
Anna
R&D Privacy Steward
Esteban
Specialist
Pfizer
Pfizer Compensation & Benefits Highlights
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Healthcare Strength — Multiple U.S. medical plan options include telehealth, comprehensive mental‑health support, fertility/family‑building benefits, transgender‑inclusive coverage, and certain Pfizer medications at no cost. A Wellbeing Wallet and wellness resources broaden the health and wellbeing offering.
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Retirement Support — A 401(k) with company matching is paired with an additional Pfizer Retirement Savings Contribution, alongside company‑paid life and disability insurance. One‑on‑one financial planning support is provided through Fidelity.
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Leave & Time Off Breadth — Paid time off spans vacation, holidays, and personal days, with additional caregiver and medical leave. U.S. parental leave commonly includes 12 weeks paid with options for additional unpaid bonding time and a return‑to‑work transition.
Pfizer Insights
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The Company
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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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Typical time on-site:
2.5 days a week
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