QC Scientist I - Andover, MA

Military Spouse Corporate Career Network • Andover, MA

4d • Onsite

About The Position

The QC Scientist I performs work to maintain Good Manufacturing Practices (cGMP)-compliant Quality Control and Stability laboratories at Pfizer’s Andover, Massachusetts site. The role includes routine bioburden and endotoxin testing of in-process and drug substance samples, supporting product dispositions through sample review and reconciliation, and assisting with laboratory inventory and other requests. The position follows site and laboratory Environment, Health and Safety requirements and applicable HR policies and colleague relations guidelines. The employee also prepares documentation such as Standard Operating Procedures (SOPs), technical reports, and project plans.

This is an on-site position with a primary first-shift schedule, Sunday through Thursday. Occasional holiday or other off-hours coverage may be required, with advance notice. Laboratory and office work involves walking, standing, and sitting during a shift, as well as reading, understanding, and following procedures and manipulating laboratory testing apparatus.

Requirements

• BA/BS degree; no specific years of experience required.
• Demonstrated manufacturing or quality 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.

Nice To Haves

• Deep understanding of microbiology testing and experience defending laboratory practices during regulatory audits.
• Proficiency in viable and non-viable environmental monitoring within pharmaceutical manufacturing.
• Solid grasp of aseptic techniques.
• Strong problem-solving skills.
• Ability to work independently and as part of a team.
• Ability to manage multiple tasks simultaneously.
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
• Curiosity about how AI tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use.

Responsibilities

• Perform tasks associated with maintaining cGMP-compliant Quality Control and Stability laboratories.
• Follow Environment, Health and Safety requirements for the site and QC laboratories.
• Perform bioburden and endotoxin testing of routine in-process and drug substance product samples.
• Support product dispositions through sample review and reconciliation.
• Support laboratory activities with routine inventory checks and ad hoc requests.
• Operate within established HR policies and basic colleague relations guidelines.
• Write SOPs, technical reports, project plans, and other documentation.

Benefits

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution.
• Paid vacation, holiday, and personal days.
• Paid caregiver/parental and medical leave.
• Medical, prescription drug, dental, and vision coverage.
• Eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of base salary.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level