Vacancy Description
Puerto Rico | Contract Opportunity | Pharmaceutical Industry
We are seeking a Regulatory QA Specialist with experience reviewing and approving documentation in a regulated pharmaceutical environment.
Key Responsibilities
- Review, verify, and approve quality and regulatory documentation.
- Ensure compliance with GMP, internal procedures, and regulatory requirements.
- Review protocols, reports, SOPs, validation documentation, and other quality records.
- Collaborate with Engineering, Manufacturing, Validation, and Quality teams to support compliance initiatives.
Qualifications
- Experience reviewing and approving documentation within the pharmaceutical or other regulated industry.
- Strong understanding of GMP documentation and...
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