BDR Pharmaceuticals International Pvt. Ltd., one of India’s fastest-growing generic pharmaceutical companies with a strong presence in regulated markets, is organizing a large-scale walk-in interview drive on 13 December 2025 (Saturday) at its state-of-the-art USFDA-approved manufacturing facility in Vadodara, Gujarat. This is a golden opportunity for freshers and experienced professionals from B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech, and ITI backgrounds to join a company known for oncology, critical care, and high-end specialty generics.
Date: 13 December 2025 (Saturday) Time: 10:00 AM – 04:00 PM Venue: BDR Pharmaceuticals International Pvt. Ltd. R.S. No. 578 & 579, Near Effluent Channel Road, Village Luna, Taluka Padra, Vadodara – 391440, Gujarat
Candidates having prior experience in USFDA, EU-GMP, or other regulated market plants will be given strong preference.
Open Positions & Department-wise Details
Quality Control – OSD
- Analyst / Officer – Sr. Officer (1–3 years) – B.Sc / M.Sc
- HPLC / LCMS / GC – Technician – Sr. Officer (3–5 years) – ITI / B.Pharm / M.Sc / M.Pharm
- Micro QC – Officer – Sr. Officer (1–3 years) – M.Sc
Production – OSD (Granulation, Coating, Compression, Packing)
- Officer – Sr. Officer (1–3 years) – B.Sc / M.Sc
- Technician – Sr. Officer (3–5 years) – ITI / B.Pharm
Quality Assurance – OSD
- Executive – Sr. Executive (APQR Reviewer) (4–6 years) – M.Sc / M.Pharm
- Executive – Sr. Executive (QMS & AQA) (6–9 years) – M.Sc / M.Pharm
- Officer – Assistant Manager (2–9 years) – M.Sc / M.Pharm / B.Tech
Engineering – OSD
- Officer – Sr. Officer (Civil / Electrical / Mechanical) (1–5 years) – B.Tech / BE / M.Tech / ITI
Environment, Health & Safety (EHS)
- Technician – Executive (3–5 years) – ITI / B.Tech / B.E / M.Tech / M.Sc
Analytical Development Lab (ADL) / Validation
- Sr. Officer – Executive (3–5 years) – M.Sc / M.Pharm / B.Pharm
GLP / Documentation
- Officer – Sr. Officer (1–3 years) – B.Sc / M.Sc
Administration
- Sr. Officer – Executive (3–5 years) – B.Com / M.Com / MBA
Key Responsibilities (Common across roles)
- Ensure compliance with cGMP, USFDA, EU, and other regulatory guidelines
- Perform routine analysis, testing, documentation, and validation activities
- Operate and maintain sophisticated instruments (HPLC, GC, LCMS, etc.)
- Participate in investigations, CAPA, and continuous improvement initiatives
- Maintain safety and environmental standards at the workplace
Required Qualifications & Skills
- Relevant degree/diploma (B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech, ITI, etc.)
- 1–9 years of hands-on experience in OSD formulation plants
- Sound knowledge of regulatory requirements (USFDA experience highly preferred)
- Good communication and documentation skills
- Willingness to work in shifts
Salary & Benefits
- Competitive salary best in the industry (based on experience and current CTC)
- Performance-linked incentives
- Group mediclaim & personal accident insurance
- Subsidized canteen & transport facility
- Provident Fund, gratuity, and leave encashment benefits
How to Apply
Walk-in directly on 13 December 2025 between 10:00 AM and 04:00 PM with updated resume, passport-size photograph, current CTC proof, and last three months’ salary slips.
Alternatively, you can apply online here: https://lnkd.in/g_ak_KVA
For any queries, contact: pritam.singha@bdrpharma.com | krishna.trivedi@bdrpharma.com
Note: This walk-in drive is only for the above-mentioned positions. For other openings, please visit BDR’s official career portal: https://bdrhrcareers.peoplestrong.com/job/joblist
Don’t miss this chance to accelerate your career with a leading oncology and critical-care focused pharmaceutical company!
