About APDM Pharmaceuticals
APDM Pharmaceuticals Private Limited, headquartered in Ahmedabad, is a global pharmaceutical service provider with a robust network of CMO, CDMO, and CRO partners. With over 100 years of combined experience in CDMO, 50 years in R&D, and decades of expertise in regulatory and QA, we specialize in managing CDO and CDMO projects, vendor audits, BA/BE monitoring, and engineering solutions.
Position Overview
Job Title: Officer / Sr. Officer / Executive / Sr. Executive – QC (Documentation & Method Validation)
Job Location: Plant, Sakodara VitL, Ahmedabad
Experience Required: 2 to 5 years
Educational Qualification: M.Sc / M.Pharm
Key Responsibilities
- Conduct and review method validations, including Assay, Dissolution, Related Compounds, and Residual Solvents.
- Prepare and finalize method validation/verification protocols for APIs and finished products.
- Develop STPs and specifications in alignment with method validation protocols.
- Review method transfer protocols, reports, and resolve queries related to Assay, Dissolution, Related Compounds, Elemental Analysis, and Residual Solvents.
- Ensure timely completion of validation/verification and method transfer activities.
- Verify the availability of essential resources like columns, impurities, reference standards, chemicals, and reagents as per MOA/protocol for exhibit batch analysis/validation/verification.
Why Join APDM Pharmaceuticals?
- Work in a global organization with a vast network of pharmaceutical service providers.
- Be part of a team with decades of R&D and regulatory expertise.
- Experience a collaborative and innovation-driven work culture.
How to Apply
Send your CV to hr@apdmpharma.com.
Application Deadline: 10th February 2025
Be a part of our mission to deliver excellence in pharmaceutical services. Apply today!
