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BDR Pharmaceuticals is expanding its team at the Luna, Padra facility and is looking for talented professionals to join their growing workforce. If you have a background in the pharmaceutical industry and experience with USFDA-regulated plants, this could be your next big career move.
Open Positions and Requirements
Analytical Method Validation & Development
We are looking for experts with 1 to 12 years of experience in the field. The ideal candidate should be highly proficient in analytical method validation using HPLC, GC, Dissolution, and various wet chemistry methods.
Production (API)
This role is suited for early-career professionals with 1 to 3 years of experience. Responsibilities include ensuring and verifying the filling of production-related documents, managing BMRs, maintaining equipment usage logbooks, and performing weighing balance verification.
Production (API)-Documentation
For more senior professionals, we have an opening requiring 7 to 8 years of experience. This role focuses on high-level documentation, including the preparation of SOPs, BMRs, and ECRs. Candidates must be experienced in handling OOS (Out of Specification), OOT (Out of Trend), and performing Gap Analysis.
Candidate Profile & Qualifications
- Education: M.Sc, B.Pharma, or M.Pharma.
- Industry: Must have a solid background in the Pharmaceutical industry.
- Preferred Experience: Candidates who have worked with regulated market products and have experience in USFDA-approved plants will be given preference.
- Location: The positions are based in Luna, Padra.
How to Apply
Ready to take the next step in your career? Please send your updated resume directly to the recruitment team:
Email: mrunali.uttekar@bdrpharma.com
Work Location: Luna, Padra
Join a team dedicated to excellence in pharmaceutical manufacturing and development!
