QC Scientist I - Andover, MA

VetJobs•Andover, MA
•$60,200 - $100,400•Onsite

About The Position

The QC Scientist I performs work to maintain cGMP-compliant Quality Control and Stability laboratories at Pfizer. The role follows site and laboratory Environment, Health, and Safety requirements; performs bioburden and endotoxin testing on routine in-process and drug substance product samples; and supports product disposition through sample review and reconciliation. The scientist also supports laboratory activities through routine inventory checks and ad hoc requests, follows HR policies and colleague-relations guidelines, and prepares documents such as SOPs, technical reports, and project plans. The primary schedule is first shift, Sunday through Thursday. Occasional holiday or other off-hours coverage may be required and will be communicated in advance. The position is on-premise in Andover, Massachusetts, and involves laboratory and office work. The annual base salary range is $60,200 to $100,400, with eligibility for Pfizer’s Global Performance Plan and a 7.5% bonus target.

Requirements

  • Bachelor of Arts or Bachelor of Science; any amount of experience is acceptable for this minimum requirement.
  • Demonstrated manufacturing or quality experience in the biotechnology or pharmaceutical industry.
  • Fundamental understanding of laboratory instrumentation functions 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 productivity; curiosity about improving outcomes with these tools 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 related documents.

Benefits

  • 401(k) plan with Pfizer matching contributions and an additional Pfizer Retirement Savings Contribution.
  • Paid vacation, holidays, and personal days.
  • Paid caregiver/parental and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Eligible to participate in Pfizer’s Global Performance Plan with a 7.5% bonus target.
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