QA Inspector

HIghly Competitive Salary
  1. Permanent
  2. Good Manufacturing Practice (GMP), Good Clinical Practice (GCP)
  3. United States
La Verne, USA
Posting date: 22 Jun 2020
SC.CN.30076

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a QA Inspector with a pharmaceutical company located in La Verne, CA.

Job Responsibilities:

  • Responsible for raw material sampling and testing coordination. Inspects incoming, intermediate, and outgoing materials for proper identification and conformance to approved specifications
  • Ensure materials are sampled and identified (quarantine, approved, on hold, or rejected) in accordance with current Good Manufacturing Practices (GMPs) requirements
  • Document, file and maintain inspection records
  • Participate in annual product visual inspection
  • Assist in maintaining the collection, retention and storage of finished product and packaging component retain samples
  • Participate in the distribution, retrieval, and filing of controlled documents (SOPs, Specifications, and Test Methods) as well as other Quality Assurance documents
  • May participate in the execution of validation and process improvement activities
  • May provide on the job training and day-to-day guidance to other non-exempt personnel

Skills and Requirements:

  • Minimum of 2 years of relevant experience
  • HS diploma required
  • Raw material and sampling are main focus

If you are having difficulty in applying or if you have any questions, please contact Catherine Nguyen at 215-531-5643.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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