Quality Specialist

Location: Sunnyvale, California, United States
Salary: competitive
Job Type: Contract
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Bio-tech Industry Client - Quality Specialist - Sunnyvale

Responsibilities:

  • Support the daily Quality Assurance activities related to GMP manufacturing for cell therapy products
  • Perform compliance review of batch production records and equipment documentation for GMP manufactured clinical products
  • Support the team with routine in-phase inspections during clinical product manufacturing
  • Responsible for authoring, reviewing and revising relevant documentation, performing quality reviews, conducting review of batch production records, conducting investigations, and assisting in hosting audits

The Ideal Candidate:

  • B.S. degree in a Life Science, ideal but not required
  • Minimum of 1-2 years' direct experience related to GMP Manufacturing in the biotechnology or pharmaceutical industry; or equivalent combination of education and experience.
  • Life Science Industry Experience (i.e. pharmaceuticals, biotech, or medical device ideal, aerospace will be acceptable)
  • Strong knowledge of GMPs
  • Excellent oral and written communication skills
  • Must be authorized to work in the U.S.

Sthree US is acting as an Employment Business in relation to this vacancy.

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