Careers at ThermoFisher Scientific


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Job ID :
Location :
Canada - Whitby
Job Description


To ensure all documentation related to the successful release of a finished product is complete and conform to all SOPs and cGMPs.

Essential Functions:

Batch Record Reviews – Quality Assurance review of executed Processing and Packaging batch records. Ensure that all documentation related to product release is assembled prior to release.
QIR Facilitation – Facilitate the investigations of IR/DRs
Release of Product – Release of bulk and Finished Product
Administration - Attend teleconference meetings with the clients. Ensure that clients are copied on batch records. Photocopying and scanning of executed batch records.
Other duties as assigned.


  • B.Sc. in chemistry, biology, life sciences or other related field.
  • 3 to 5 years experience in the pharmaceutical industry, preferably in a QA function.
  • Experience with Microsoft Word and Excel.
  • Excellent interpersonal oral and written communication skills.
  • Working knowledge of SAP is an asset.
  • Ability to work rotating shifts (Midnight, Afternoon and Day) is required.

Thermo Fisher Scientific  is an equal opportunity employer and is committed to the principle of diversity and is particularly interested in receiving applications from a broad spectrum of people. Accommodations for job applicants with disabilities are available upon request.

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