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Quality Assurance Senior Associate

Thousand Oaks, CA
“This Company requires all staff, staff augmentation external workers, and certain other external workers, in the United States and Puerto Rico vaccinated from COVID 19 as a condition of assignment at this company. In accordance with applicable law, this company will provide reasonable accommodations staff augmentation external workers qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship this company, its operations, or its staff.”                                                        

Top 3 Must Have Skills                    
  • Must have experience with GMP processes and documentation. Without that fundamental skillset the training for document review tasks, aseptic filling support, and defect inspection will have no foundation.
  • Must be able to methodically and meticulously inspect product containers for defects and review both batch record documentation and exception records for accuracy and completeness.
  • Must be able to work in a team with shifting priorities and shifting responsibilities, such that the team members must be confident verbal communicators able to discuss responsibilities, divide them, reassess them, and potentially reassign them throughout the day or week.
Day to Day Responsibilities:                        
  • Primary responsibilities will include review and approval of GMP manufacturing batch records, visual inspection of filled product containers, and generation and compilation of quality data and reports (e.g. lot track/trace, deviations). Individual will also assist with procedure reviews and initiation of deviation reports.

"This posting is for Contingent Worker, not an FTE"

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