We’re looking for a QA Specialist to support our Bulk Drug Substance facility at ADMF, ensuring the highest standards of GMP compliance across manufacturing, testing, documentation, and product disposition
Job Summary
We’re looking for a QA Specialist to support our Bulk Drug Substance facility at ADMF, ensuring the highest standards of GMP compliance across manufacturing, testing, documentation, and product disposition.
This role offers the opportunity to make a meaningful impact in a fast-paced biologics environment where quality truly matters.
Join a high-impact QA team where your expertise directly safeguards the quality, safety, and availability of life-changing biologic medicines for patients worldwide.
Matching Summary
We’re looking for a QA Specialist to support our Bulk Drug Substance facility at ADMF, ensuring the highest standards of GMP compliance across manufacturing, testing, documentation, and product disposition.
Skills & Requirements
Must-have
cGMP compliance oversight
Quality Management System maintenance
Batch record review and approval
Inspection readiness support
Quality risk assessment participation
Supplier management activities
Quality metrics development and reporting
Nice-to-have
Strong communication and presentation skills
Ability to work in international matrix environment
Leadership presence with cross-functional influence
Key Requirements
Experience in pharmaceutical or biotech industry
Degree in Pharmacy, Biology, Biotechnology, Engineering or relevant scientific discipline