BDR Pharma Hiring in Luna Padra – Analytical Method Validation & API Production Specialists | January 2026
BDR Pharmaceuticals, a leading pharmaceutical manufacturer, is expanding its team at the Luna, Padra facility and invites talented professionals to join their world-class operations. If you have experience in USFDA-regulated pharmaceutical plants and expertise in analytical methods or API production, this is an excellent opportunity to advance your career.
About BDR Pharmaceuticals
BDR Pharmaceuticals is committed to manufacturing high-quality pharmaceutical products with a strong focus on regulatory compliance, innovation, and excellence. The company operates state-of-the-art facilities that adhere to stringent USFDA standards, providing professionals with exposure to global pharmaceutical manufacturing practices.
Open Positions
1. Analytical Method Validation & Development
Experience: 1 to 12 years
Key Responsibilities:
• Conduct analytical method validation using HPLC, GC, Dissolution, and various wet chemistry methods
• Develop and validate analytical procedures for pharmaceutical products
• Ensure compliance with regulatory requirements and pharmacopeial standards
• Perform method transfer and troubleshooting activities
Qualification: M.Sc, B.Pharma, or M.Pharma
2. Production (API) – Junior Level
Experience: 1 to 3 years
Key Responsibilities:
• Ensure and verify the filling of production-related documents
• Manage Batch Manufacturing Records (BMRs)
• Maintain equipment usage logbooks
• Perform weighing balance verification and calibration activities
• Follow GMP practices and maintain production area cleanliness
Qualification: M.Sc, B.Pharma, or M.Pharma
3. Production (API) – Documentation
Experience: 7 to 8 years
Key Responsibilities:
• Prepare and review SOPs, BMRs, and ECRs (Engineering Change Requests)
• Handle Out of Specification (OOS) and Out of Trend (OOT) investigations
• Perform Gap Analysis for production documentation
• Ensure documentation compliance with regulatory standards
• Coordinate with cross-functional teams for documentation updates
Qualification: M.Sc, B.Pharma, or M.Pharma
Preferred Candidate Profile
• Educational Background: M.Sc, B.Pharma, or M.Pharma
• Industry Experience: Pharmaceutical industry background is mandatory
• Regulatory Exposure: Experience in USFDA-approved plants will be given preference
• Technical Skills: Proficiency in analytical instruments, documentation, and GMP practices
• Work Location: Luna, Padra, Gujarat
How to Apply
Interested candidates meeting the above criteria should send their updated resume directly to the recruitment team:
Email: mrunali.uttekar@bdrpharma.com
Work Location: Luna, Padra, Gujarat
Join BDR Pharmaceuticals and become part of a team dedicated to pharmaceutical excellence and innovation. This is your opportunity to work in a USFDA-regulated environment and contribute to manufacturing high-quality pharmaceutical products.
