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Quality Assurance Specialist

Mallinckrodt
Port Allen, LA Full Time
POSTED ON 4/22/2025
AVAILABLE BEFORE 5/21/2025

This position requires a strong understanding of cGMPs, OSHA, EPA, and FDA regulations. The successful candidate will have experience working in a regulated environment and be able to collaborate with various organizational levels.

Key Responsibilities

  1. Perform chemical analysis of raw material, in-process materials, finished drug product, stability, validation, and R&D samples in accordance with regulatory requirements
  2. Collect, handle, and document raw materials, chemical reagents, laboratory standards, and sample vessels in accordance with regulatory requirements
  3. Calibrate and perform preventative maintenance of analytical instruments in accordance with regulatory requirements
  4. Review other analysts' work and perform routine housekeeping activities

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