Assistant pharmacist
Carmona
Job Description
Posted on 4 May 2026- Liaising with regulatory authorities to obtain necessary approvals for new and existing pharmaceutical products
- Preparing and submitting regulatory submissions, including new drug applications, variations, and renewals
- Monitoring changes in regulatory guidelines and ensuring our products and processes remain compliant
- Providing regulatory guidance and support to cross-functional teams, including R&D, manufacturing, and quality assurance
- Maintaining comprehensive regulatory documentation and records
- Staying up-to-date with industry trends and best practices in regulatory affairs
- Graduate of BS Pharmacy
- Proven experience in compliance management within the pharmaceutical or biotech industry.
- Strong knowledge of FDA regulations, including 21 CFR Part 11, Good Manufacturing Practices (GMP), and Good Clinical Practice (GCP).
- Experience with clinical trials oversight and documentation.
- Familiarity with research processes and quality assurance protocols.
- Excellent project management skills with the ability to coordinate multiple initiatives simultaneously.
- Strong analytical skills with attention to detail in documentation review and process evaluation.
Work location
CARMONA, CAVITE
Remarks
No additional remarks
Apply now
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