Qc Technical Data Reviewer

Pfizer Com Ec

Rocky Mount, North Carolina, US
Base: $32.01 to $53.35 ph; bonus/equity: not speci...
On premise
Qc chemistry laboratories data review
Review testing documentation
Review electronic data and audit trails
Pfizer is seeking a QC Technical Data Reviewer for their Rocky Mount, North Carolina facility, responsible for ensuring the quality and compliance of pharmaceutical products. The ideal candidate should have significant experience in quality assurance, particularly in a cGMP environment, and possess strong analytical and organizational skills

Job Summary

  • Your expertise in quality assurance will ensure that our products meet the highest standards, ultimately benefiting those who rely on our medications.
  • Serve as a key resource and potentially lead lower levels within your area of expertise.
  • We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.

Matching Summary

Match Score: 85

Pfizer is seeking a QC Technical Data Reviewer for their Rocky Mount, North Carolina facility, responsible for ensuring the quality and compliance of pharmaceutical products. The ideal candidate should have significant experience in quality assurance, particularly in a cGMP environment, and possess strong analytical and organizational skills.

Salary

Base: $32.01 to $53.35 per hour; Bonus/Equity: Not specified; 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, and health benefits to include medical, prescription drug, dental and vision coverage

Skills & Requirements

Must-have

  • QC Chemistry laboratories data review
  • Review testing documentation
  • Review electronic data and audit trails
  • Adhere to Pfizer standards and guidelines
  • Quality in clinical and commercial drug batches
  • Evaluate and review batch records
  • Manage batch disposition
  • Maintain documentation
  • Review and approve investigations
  • Review and approve change control activities
  • Perform and document qualitative or quantitative assays
  • Review sterility and potency assays
  • Maintain records
  • Oversee quality operations
  • Lab safety and compliance
  • Safe use of chemicals
  • Recognition of DEA, FDA, OSHA and ICH guidelines
  • Hands-on analytical testing experience
  • GMP environment experience
  • cGMP environment experience
  • Proficiency in applicable computer software
  • Personal leadership and accountability
  • Operational regard for customer needs
  • Strong organizational skills
  • Ability to multi-task
  • Good communication skills
  • Basic computer skills in Microsoft Office

Nice-to-have

  • Experience in parenteral drug product manufacturing
  • Experience training junior staff
  • Experience mentoring junior staff
  • Proficiency in Quality Tracking System
  • Proficiency in Laboratory Information Management System
  • Proficiency in Application & Products
  • Proficiency in Lot Review Tracking systems
  • Excellent attention to detail
  • Strong interpersonal skills
  • Ability to adapt to changing priorities
  • Familiarity with common AI tools
  • Curiosity for learning AI tools

Key Requirements

  • HS Diploma or GED and 10 years of relevant experience
  • Associate’s degree with 8 years of experience
  • Bachelor's degree with 6 years of experience
  • Experience in quality functions of the pharmaceuticals industry
  • Permanent work authorization in the United States

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter