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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 Skill Sets:  
         
  • Technical writing experience (i.e. deviation records, CAPA records, controlled documents)
  • Excellent verbal and written cross functional communication skills
  • Must have biotech/pharma manufacturing, quality assurance, or quality control experience
Day to Day Responsibilities:                    
Purposeful presence on the manufacturing floor (80% of working time spent on MFG floor in controlled, classified cell culture and protein purification areas).
  • Batch record review
  • SOP and MP revision approval
  • work order approval
  • quality approval of deviations and CAPAs
  • Safety auditing and observational work
  • GEMBA walks
"This posting is for Contingent Worker, not an FTE"

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