About this opportunity
Nivagen Pharmaceuticals, Inc. lists this Senior QA/QMS Specialist - Deviations & Investigations opportunity in sacramento, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Nivagen Pharmaceuticals, Inc. in Sacramento, CA seeks a QA/QMS Senior Specialist - Deviations & Investigations to lead deviation management across sterile GMP manufacturing.
You will initiate, investigate, and close deviations per FDA/cGMP requirements, serving as the central contact for lifecycle management with cross-functional teams. Must have strong investigative writing, familiarity with TrackWise or Veeva QMS, and knowledge of 21 CFR Parts 210–212.
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Worksite address
sacramento, CA, 95828, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.