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Pfizer
Pfizer
H1B Visa SponsorConsultingMarketingPharmaceuticals
Pfizer is a global pharmaceutical company focused on developing and providing medicines and healthcare services that support health throughout life. Its work spans scientific innovation and access to safe, effective, and affordable treatments, with a particular emphasis on advancing therapies for cancer and other significant health conditions. The company’s profile may be relevant to professionals exploring careers in pharmaceutical research, healthcare, and related commercial functions.
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Senior Associate Scientist, GMP Investigations and Compliance

Support Pfizer’s medicines and vaccines by strengthening GMP investigations and compliance across R&D sites. Write investigations, assist with audits, and use quality data to drive improvements.

USUnited StatesMAMassachusettsMOMissouri
$68,600 – $114,300 / year
HybridFull-timeSeniorEnglish RequiredCompliance

Description

  • Prepare clear, timely investigations using Pfizer quality systems.
  • Check investigations against applicable quality and compliance standards.
  • Encourage consistent use of root cause analysis and human error reduction methods.
  • Assist with internal and external audits and inspections, coordinating requests and responses.
  • Assess compliance with global procedures.
  • Review compendia and regulatory requirements.
  • Take part in internal quality forums.
  • Evaluate investigation, audit, and inspection data to identify, recommend, and implement improvements.
  • Select solutions for moderately complex issues and follow procedures under general guidance.
  • Help meet work group objectives and collaborate with colleagues.
  • Manage priorities to meet project deadlines and contribute as a team member.

Requirements

  • Bachelor’s degree in microbiology, molecular biology, biochemistry, or a related field and at least three years of GMP microbiology laboratory experience; alternatively, an MBA or MS and at least one year of experience.
  • Advanced technical writing ability.
  • Strong documentation skills and careful attention to detail.
  • Experience working in Good Manufacturing Practices (cGMP) settings.
  • Experience with GMP microbiology investigations.
  • Experience with laboratory data platforms such as LIMS, eQMS, and GDMS.
  • Ability to work effectively with peers and leaders on cross-site, multidisciplinary teams.
  • Ability to find relevant information in scientific literature.
  • Ability to manage timelines and deliverables independently.
  • Strong organizational skills and demonstrated attention to detail.
  • Experience using common AI tools, including generative tools such as ChatGPT or Microsoft Copilot, to solve problems and improve productivity.
  • Curiosity about how AI tools can improve outcomes, along with understanding of responsible AI practices, including risk management and ethical use.
  • Must be authorized to work in the United States for any employer.
  • U.S. work visa sponsorship is unavailable for this role, now and in the future.
  • Permanent U.S. work authorization is required.

Benefits

  • 401(k) plan with Pfizer matching contributions.
  • Additional Pfizer retirement savings contribution.
  • Paid vacation, holidays, and personal days.
  • Paid caregiver, parental, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Relocation support may be offered depending on business needs and eligibility.
  • May participate in Pfizer’s Global Performance Plan, with a bonus target of 7.5% of base salary.

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