Document Reviewer Ii - Qa- Afternoon Shift

Thermo Fisher Scientific UK

Ontario, Canada
Base: $50,800.00–$76,150.00; bonus/equity: not spe...
Bachelor of science in chemistry
3 years pharmaceutical analytical experience
Good manufacturing practices (gmp) knowledge
The role is responsible for reviewing all data, lab notebooks, and Certificates of Analysis generated in the Laboratory

Job Summary

  • The role is responsible for reviewing all data, lab notebooks, and Certificates of Analysis generated in the Laboratory.
  • Candidates must verify the integrity and traceability of all data reported in accordance with Good Manufacturing Practices standards.
  • This position requires a Bachelor of Science in Chemistry or related science with at least three years of pharmaceutical analytical development experience.

Matching Summary

The role is responsible for reviewing all data, lab notebooks, and Certificates of Analysis generated in the Laboratory.

Salary

Base: $50,800.00–$76,150.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Bachelor of Science in Chemistry
  • 3 years pharmaceutical analytical experience
  • Good Manufacturing Practices (GMP) knowledge
  • HPLC and Gas Chromatography understanding
  • Empower LIMS Nugensis Trackwise software

Nice-to-have

  • Strong organizational skills and detail oriented
  • Ability to meet deadlines and prioritize
  • Proactive problem solving and communication
  • Openness to change and team adaptation

Key Requirements

  • Bachelor of Science in Chemistry
  • Minimum 3 years pharmaceutical analytical experience
  • Knowledge of FDA and ICH requirements

Work Rights

Not specified

Tailored Resume

Cover Letter