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Quality Assurance Specialist

Company: Cameron Craig Group
Location: Jackson
Posted on: November 22, 2021

Job Description:


The QA Specialist will review manufacturing batch records, testing results and deviation reports for compliance with cGMP and company procedures with minimal supervision. To release products, drug product components and container-closures. To review and write cGMP procedures under supervision. To report periodic quality metrics.


  • Review manufacturing batch records, testing results and deviation reports
  • Interact with other departments to address review observations
  • Use of Quality related electronic systems (for example, LN, QIS, LIMS)
  • Release drug product, drug product components and container-closures
  • Interact with customers on batch record reviews and batch releases
  • Attend department meetings on batch record review and releases
  • Maintain and report quality metrics on batch record review and releases
  • Review and write standard operating procedures
  • Review quality system documents (change controls, validation, complaints)
  • Review master batch records and maintain records
  • Process, investigate and follow-up on product complaints
  • Perform other tasks as requested by management.

    Requirements:
    Bachelor's Degree (BA or BS), preferably in a Natural Science, is required. A minimum of 3 years of relevant experience in the pharmaceutical industry is required. Must be eligible to work in the USA
    --

Keywords: Cameron Craig Group, Brick , Quality Assurance Specialist, Other , Jackson, New Jersey

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