Astrixposted about 1 month ago
$22 - $23/Yr
Paris, KY
Professional, Scientific, and Technical Services

About the position

Our Client, a Fortune 500 leader, is hiring for Quality Assurance Associate. Be part of a team setting science in motion across the biopharma, healthcare and advanced technologies industries. Are you ready to make a global impact? Join us now!

Responsibilities

  • Issuance of controlled manufacturing and testing documents to Manufacturing and Quality Control as per the production schedule.
  • Issuance of controlled labels used for labelling finished goods and other related samples.
  • Monitor the equipment program including calibration and preventative maintenance timelines and complete quality assurance sign-off for equipment workorders.
  • Coordinate the release of raw materials after completion of review and approval of supporting documentation including supplier and quality control testing records.
  • Conduct reconciliation, filing and archiving all quality-controlled records. The store completed documents in the appropriate data files and coordinated off-site document storage with third party as necessary.
  • May provide batch record review support.
  • Writing and revising SOPs as part of process improvement initiatives or as needed to support the department.
  • Coordination of document control activities and delegating with other quality coordinators to drive workload completion in the direction of quality management.

Requirements

  • BA/BS in chemistry or science-related field preferred, or equivalent from two-year college or technical school.
  • A minimum of 2 years of experience in Quality including cGMP and ISO standard.
  • Experience of cGMP and MS Word, PowerPoint and Excel.
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