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Job ID :
62465BR
Location :
Canada - Whitby
:
Job Description

Summary:

The purpose of this one-year contract is to write analytical validation protocols and reports.

Essential Functions:

  • Prepare with supervision analytical protocols and reports with high quality and deliver within agreed schedules and complete all work according to current SOPs and various guidelines from regulatory agencies.
  • Communicate and coordinate with all sites to complete and revise protocols and reports on time.
  • Other duties as required.
  • May be essential to perform alternating or rotating shift work.

Qualifications:

  • Bachelor of Science (B.Sc.) or Master of Science (M.Sc.) in Chemistry or related science.
  • Minimum 2 years pharmaceutical industry experience, preferably in an analytical development function.
  • Basic understanding of common analytical technologies (e.g. High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectroscopy, titration)
  • Basic understanding of Good Manufacturing Practices, International Conference on Harmonization (ICH) and United States Food & Drug Administration (FDA) requirements.
  • Basic computer proficiency with Microsoft Office programs.
  • Ability to meet deadlines and prioritize.
  • Proficiency with the English language.
  • Excellent written and oral communication skills with strong attention to detail.




Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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