BDR Pharmaceuticals International Pvt. Ltd., a leading player in the Indian pharmaceutical industry with a strong focus on Active Pharmaceutical Ingredients (APIs), peptides, and regulated market products, is actively hiring talent for its state-of-the-art Luna plant near Vadodara, Gujarat. The company, known for its USFDA-approved facilities and expertise in complex generics, is inviting eligible candidates for a walk-in interview on February 14, 2026.
This is a great opportunity for professionals with 2–12 years of experience in R&D, Analytical Development, and Regulatory Affairs to join a dynamic team driving innovation in API manufacturing.
About BDR Pharmaceuticals
BDR Pharmaceuticals specializes in developing and manufacturing high-quality APIs for oncology, cardiology, anti-diabetic, and other therapeutic segments. With manufacturing sites in Gujarat and a commitment to global regulatory standards, the company emphasizes quality, compliance, and cutting-edge research.
Open Positions and Experience Requirements
The hiring drive targets multiple roles across key departments at the Luna plant:
R&D Department (API)
- API Synthesis: 2–4 years
- Peptide Synthesis: 2–4 years
- Process Development Lab: 2–4 years
- Impurities Lab: 2–4 years
- Polymorphism: 2–4 years
Regulatory Affairs (RA) Department (API)
- Regulatory Affairs (API): 4–11 years
Analytical Development & Impurities (ADL) Department
- Analytical Method Validation (LCMS): 4–5 years
- Analytical Method Development & QMS: 2 years (likely 2–4+ based on context)
- Analytical Synthesis Method Validation & QMS: 9–12 years
Candidates with experience in regulated market products (US/EU) and USFDA-approved plants are strongly preferred.
Roles and Responsibilities
Responsibilities vary by role but generally include:
- Developing and optimizing synthetic routes for APIs and intermediates
- Conducting peptide synthesis and related process scale-up
- Handling polymorphism studies, impurity profiling, and characterization
- Analytical method development, validation (including LCMS), and troubleshooting
- Ensuring compliance with QMS, ICH guidelines, and regulatory requirements
- Preparing regulatory dossiers and supporting filings for international markets
- Working in lab environments focused on innovation and quality
Required Qualifications and Skills
- M.Sc./M.Pharm/Ph.D. in Organic Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, or related fields
- Hands-on experience in API R&D, analytical techniques (HPLC, LCMS, GC, etc.), or regulatory submissions
- Knowledge of cGMP, GLP, ICH, and USFDA guidelines
- Strong problem-solving, documentation, and teamwork abilities
- Experience in regulated markets is highly desirable
Salary and Benefits
While exact figures depend on the role, experience, and negotiation, typical salary ranges for these positions in Gujarat-based API companies are:
- Officer/Sr. Officer (2–5 years): ₹4–8 LPA
- Executive/Asst. Manager (4–8 years): ₹6–12 LPA
- Manager-level (9+ years): ₹12–20+ LPA
Benefits often include performance incentives, health insurance, provident fund, transport facilities (common for plant locations), and professional growth opportunities in a USFDA-compliant environment.
How to Apply
Attend the walk-in interview:
- Date: February 14, 2026 (Saturday)
- Time: 10:00 AM to 4:00 PM
- Venue: BDR Lifesciences Pvt. Ltd., RS No. 578 & 579, Near Effluent Channel Road, Village: Luna, Taluka: Padra, District: Vadodara – 391440, Gujarat
Contact Person: Mrunal Uttekar Email: mrunal.uttkar@bdrpharma.com
Note: This walk-in is specifically for the mentioned openings at the Luna plant. For other roles across BDR, visit the official career page: https://bdhrcareers.peoplestrong.com/job/joblist
Bring updated resume, educational certificates, experience letters, and recent passport-size photographs.
