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 Quality Systems.
- 5–10 years of experience preferred; candidates with 2–3 years of relevant experience will also be considered.
Compensation: $30–$45/hour, based on experience.
About the Opportunity
These are contract positions supporting leading pharmaceutical manufacturing operations in Puerto Rico. If you have experience working in regulated environments and are looking for your next challenging project, we'd love to hear from you.