Quality Control Raw Materials Sampling Associate
PfizerAbout the role
Use Your Power for Purpose
Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.
The Quality Control (QC) Analytical group is seeking a highly motivated candidate to support Good Manufacturing Practices (GMP) sampling and analytical testing of raw materials at the Andover, MA site. The candidate will perform sampling, testing, and support activities for raw materials, attend meetings, and participate in continuous improvement activities
What You Will Achieve
In this role, you will:
Perform Raw Material Sampling in the GMP warehouse to support clinical and commercial manufacturing operations.
Perform Daily Sanitization of ISO classified Sampling Areas.
Perform and Review Appearance, Gas, and Raman Spectroscopy testing on Raw Materials.
Participate in continuous improvement culture within sampling areas. Identify opportunities for improvements and utilize site continuous improvement tools.
Plan and prioritize assignments to meet department and site goals.
Record and maintain all related data and records in compliance with Current Good Manufacturing Practices (cGMP) and quality procedures.
Perform work in a manner consistent with company safety policies and procedures.
Participate in company culture based programs.
Perform additional tasks as needed in the QC Analytical Department
Here Is What You Need (Minimum Requirements)
BA/BS with any years of experience
Demonstrated experience in manufacturing quality or engineering experience in the biotech or pharmaceutical industry
Fundamental understanding of laboratory instrumentation function and analytical method troubleshooting
Excellent oral, written, and interpersonal communication skills
Knowledge of Microsoft Office applications, specifically Word and Excel
Ability to perform complex mathematical problems and data analysis
Bonus Points If You Have (Preferred Requirements)
QC laboratory experience within a GMP laboratory, including: QC analytical testing, Raman Spectroscopy testing, sampling raw materials preferred.
Understanding of GMP concepts preferred.
Experience with Labware LIMS preferred.
PHYSICAL/MENTAL REQUIREMENTS
5 to 8 hours walking, lifting, moving materials in the warehouse.
Occasional lifting of 50 - 100 pounds (can be assisted if needed)
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required to support staff and operations.
Other Job Details:
Last day to Apply: June 3, 2026
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Suns
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s