Regulatory Compliance Associate

4 days ago


Bothell, Washington, United States Omni Inclusive Full time
Key Responsibilities
  • Review of cGMP Controlled Documents, including SOPs and batch records, to ensure compliance with approved procedures.
  • Conducting quality walk-throughs of production, testing, and warehouse locations to identify potential issues.
  • Executing quality operations in support of manufacturing and logistics, providing guidance during GMP events and deviation investigations.
  • Supporting the batch disposition process by ensuring accurate completion of required documents.

The ideal candidate will possess strong computer skills, attention to detail, and effective communication skills.



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