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
Knowledge of hplc and gas chromatography
The role is responsible for reviewing all data, lab notebooks, and Certificates of Analysis generated in the laboratory to verify integrity and traceability

Job Summary

  • The role is responsible for reviewing all data, lab notebooks, and Certificates of Analysis generated in the laboratory to verify integrity and traceability.
  • Candidates must possess a Bachelor of Science in Chemistry and a minimum of three years of previous pharmaceutical analytical development experience.
  • The position requires strict compliance with Good Manufacturing Practices (GMP) and the ability to work alternating or rotating afternoon shifts.

Matching Summary

The role is responsible for reviewing all data, lab notebooks, and Certificates of Analysis generated in the laboratory to verify integrity and traceability.

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
  • Knowledge of HPLC and Gas Chromatography
  • Proficiency with Empower LIMS and Trackwise
  • Strict adherence to Good Manufacturing Practices

Nice-to-have

  • Strong organizational and detail-oriented skills
  • Excellent written and oral communication
  • Ability to prioritize and meet deadlines
  • Proactive problem-solving mindset
  • Willingness to work rotating shifts

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter