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Job ID :
62037BR
Location :
Canada - Whitby
:
Job Description

Summary:

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.

Qualifications:

  • 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 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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