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Biotechnology Validation Expert

2 weeks ago

London, Ontario, Canada Flippa Full time
Job Responsibilities:
As a Validation Engineer/Specialist, you will be responsible for writing C/Q/V documents following established standards and templates. This includes creating WIFI and Clean Steam SOPs, Performance Qualification Protocols, and Summary Reports. Your expertise in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA will enable you to deliver high-quality results and support our teams of industry subject matter experts and thought leaders.