QA Specialist (ID#014)

Miami, Florida

Post Date: 07/06/2017 Job ID: JN -072017-8986 Industry: Quality Assurance Specialist
A Pharmaceutical company in Miami is looking for a QA Specialist to join the team for a full time, permanent position.

QA Specialist Responsibilities:
  • Review of quality and manufacturing deviations and complaints, SOPs, and change control documents.
  • Handles investigations and audits.
  • Ensure cGMP compliance at all times.
  • Reporting of investigations, deviations, and audits.
  • Writes and reviews SOPs.
  • Reviews data to determine trends.
  • Manages and ensures timely completion of CAPA commitments.
  • Implements Change controls.
  • Generate and report complaint metrics for meetings and Annual Product Reviews
  • Complaint handling.
  • Develop Monthly reports.

QA Specialist Requirements:
  • Bachelor Degree is required
  • 3+ years of experience as a QA Specialist within cGMP regulated industry.
  • Must have Pharmaceutical/Vitamin/Supplement industry experience.
  • Experience with CAPA, Investigations, and deviations.
  • Must have experience writing AND reviewing SOPs
  • Strong written and verbal English communication skills.
  • Strong knowledge of Microsoft office (Excel/Word).

EOE/ADA
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