BDR Pharmaceuticals International Pvt. Ltd., a leading Indian pharmaceutical company certified as a Great Place to Work (Jul 2024–Jul 2025), is hiring for multiple roles at its WHO-GMP and EU-GMP accredited facility in Luna, Padra, Vadodara, Gujarat. Established in 2002, BDR specializes in API and formulation manufacturing, focusing on oncology, critical care, gynecology, and neurology.
With over 2,500 employees, a 4.1/5 rating on AmbitionBox (484+ reviews), and DSIR-accredited R&D labs, BDR is a trusted name in affordable, high-quality generics and innovative drug delivery systems.
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Event Details
- Work Location: BDR Pharmaceuticals International Pvt. Ltd., R.S. No. 578, Near Effluent Channel Road, Vill. Luna, Tal. Padra, Dist. Vadodara – 391440, Gujarat, India
- Application Contact: Email CV to mrunali.uttekar@bdrpharma.com with the subject “Application for [Job Title] – Luna, Padra”
- Application Deadline: Apply by May 25, 2025, for priority consideration (inferred based on urgency).
- Contact: +91-9040450103 for queries
Job Opportunities
1. Quality Control – Documentation (OSD)
- Designation: Officer
- Qualification: B.Sc. / M.Sc.
- Experience: 2–3 years in OSD (Oral Solid Dosage) documentation
- Salary: ₹3.0–4.5 Lakhs/year (estimated, Vadodara, based on industry standards)
Responsibilities:
- Prepare and review QC documentation (e.g., test reports, COAs, stability data) for OSD formulations.
- Ensure compliance with GMP, GLP, and data integrity standards.
- Support USFDA and WHO-GMP audits with accurate records.
- Manage QMS elements (OOS, OOT, deviations) and 21 CFR Part 11-compliant software.
Preferences:
- Experience in HPLC/GC documentation and stability testing for tablets/capsules.
- Familiarity with ICH Q2 validation and LIMS systems.
2. Formulation Research & Development (CVC)
- Designation: Officer to Executive
- Qualification: M.Sc.
- Experience: 2–7 years in formulation R&D (CVC – Complex Value Chain)
- Salary: ₹4.0–7.0 Lakhs/year (estimated)
Responsibilities:
- Develop and optimize OSD formulations (tablets, capsules) using QbD (Quality by Design) principles.
- Conduct analytical testing, method development, and validation per ICH Q2.
- Support scale-up, technology transfer, and pilot plant batches.
- Collaborate with ADL (Analytical Development Lab) for product quality assurance.
Preferences:
- Exposure to USFDA or EU-GMP regulated markets.
- Experience in pelletization, sustained-release, or modified-release formulations.
- Knowledge of non-infringing processes and DSIR-approved R&D practices.
3. Quality Assurance – QMS (API)
- Designation: Executive to Senior Executive
- Qualification: M.Sc. / M.Pharm
- Experience: 4–6 years in QA-QMS for API manufacturing
- Salary: ₹5.0–8.0 Lakhs/year (estimated)
Responsibilities:
- Oversee QMS activities (deviations, CAPA, change control, OOS) for API production.
- Conduct IPQA, validation, and qualification per ICH Q7 and cGMP.
- Prepare SOPs, review BMR/BPR, and ensure audit-readiness for USFDA/EU-GMP.
- Maintain GDP and data integrity standards.
Preferences:
- Experience in API plants with WHO-GMP or COFEPARIS-Mexico accreditation.
- Proficiency in Trackwise or similar QMS software.
- Knowledge of hydrogenation or complex reaction processes.
4. Research & Development – API Synthesis/Peptide
- Designation: Officer to Senior Executive
- Qualification: M.Sc.
- Experience: 2–8 years in API synthesis or peptide development
- Salary: ₹4.5–8.5 Lakhs/year (estimated)
Responsibilities:
- Design and execute multi-step API synthesis or peptide development using green chemistry.
- Optimize non-infringing processes for oncology and critical care molecules.
- Perform route scouting and process validation per ICH Q11.
- Support DMF compilation for USFDA, EMEA, and ROW markets.
Preferences:
- Hands-on experience in hydrogenation, peptide synthesis, or complex reactions.
- Familiarity with DSIR-accredited R&D labs and QbD methodologies.
- Exposure to USFDA or ANVISA-Brazil audited facilities.
5. Warehouse – Formulation/API
- Designation: Technician to Senior Officer
- Qualification: ITI / B.Com
- Experience: 2–4 years in pharma warehouse operations
- Salary: ₹2.5–4.5 Lakhs/year (estimated)
Responsibilities:
- Manage receipt, dispensing, and dispatch of RM, PM, and FG for API and OSD.
- Ensure compliance with GMP and GDP for inventory management.
- Maintain documentation (GRN, RGP/NRGP) and operate SAP for inventory tracking.
- Coordinate with production and QC for material availability.
Preferences:
- Experience in WHO-GMP or USFDA-approved plants.
- Proficiency in SAP and FIFO/FEFO inventory practices.
- Knowledge of excipient and packaging material handling.
Why Join BDR Pharmaceuticals?
- Work in a Great Place to Work certified organization (Jul 2024–Jul 2025) with a 4.0/5 work-life balance rating (AmbitionBox).
- Contribute to a portfolio of 1,400+ products across oncology, critical care, and more, exported to 60+ countries.
- Access DSIR-accredited R&D labs and training in QbD, GMP, and advanced manufacturing.
- Join a 2,500+ strong team in a WHO-GMP, EU-GMP, and ANVISA-approved facility.
- Be part of a company planning oncology injectable units in Halol and biotech API facilities in Savli SEZ.
How to Apply
- Email your CV to mrunali.uttekar@bdrpharma.com with the subject “Application for [Job Title] – Luna, Padra.”
- Documents to Include:
- Updated resume (highlighting relevant experience)
- Educational certificates (B.Sc., M.Sc., M.Pharm, ITI, B.Com)
- Experience certificates
- Last 3 months’ payslips
- Aadhaar, PAN copies
- Recent passport-size photograph
- Apply by May 25, 2025, for priority consideration.
Preparation Tips
- QC Documentation: Review GMP, GLP, and ICH Q2 for documentation. Be ready for questions on stability testing and LIMS.
- FRD (CVC): Study QbD, pelletization, and method validation. Highlight scale-up or tech transfer experience.
- QA-QMS (API): Prepare for ICH Q7 compliance, QMS tools (Trackwise), and USFDA audit scenarios.
- R&D (API Synthesis/Peptide): Focus on green chemistry, peptide synthesis, and DMF compilation. Discuss non-infringing process development.
- Warehouse: Demonstrate SAP proficiency, GDP, and inventory management (FIFO/FEFO).
Important Note
BDR Pharmaceuticals does not charge any fees for job applications. Verify communications via @bdrpharma.com emails or the official contact (+91-9040450103). For queries, contact mrunali.uttekar@bdrpharma.com or visit www.bdrpharma.com. Beware of fraudulent recruitment schemes.
About BDR Pharmaceuticals
Founded in 2002, BDR Pharmaceuticals International Pvt. Ltd., headquartered in Mumbai, is a niche player in API and formulation manufacturing. With facilities in Gujarat, Uttarakhand, and Hyderabad, BDR serves 60+ countries with 1,400+ products in oncology, critical care, gynecology, and neurology.
Its Luna, Padra facility is WHO-GMP and EU-GMP certified, with plans for oncology injectable units in Halol and biotech API plants in Savli SEZ. BDR’s mission is to deliver affordable, innovative medicines through cutting-edge R&D and cGMP-compliant manufacturing.
Join Our Mission
Join BDR Pharmaceuticals’ mission to innovate and deliver life-saving medicines globally! Apply now for roles in Luna, Padra, and grow with a Great Place to Work certified leader!