Actalent in Irvine, CA is seeking a Quality Technical Writer to support a quality and investigations team by drafting deviation reports, root cause analyses, and CAPA documentation within a regulated laboratory environment.
You will translate complex technical information into clear, compliant documentation, collaborate with quality assurance, investigations, and technical writing teams, and contribute to the burndown of open investigations while leveraging SAP documentation systems.
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GMP Quality Technical Writer - CAPA & Investigations
Actalent · Irvine, CA, USA ·
- Job type:
- Full Time