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Quality Assurance Senior Associate

West Greenwich, RI

“This Company requires all staff, staff augmentation external workers, and certain other external workers, in the United States and PuertRictbe 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:                
  • Deviation experience
  • Track wise System
  • GMP
  • Any experience with working in manufacturing or quality lab setting in the past (3+ years)
Day Day Responsibilities:                            
Quality oversight to QC Labs, deviation write up and closure, CAPA support.

Summary
Primary responsibilities - Quality oversight of Quality Control laboratories activities equipment, systems and process with alignment into the company Quality Systems.
Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.
Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA)
Skills: ; quality assurance or quality control laboratory testing experience in the pharmaceutical or medical device industry

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

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