BDR Pharmaceuticals Walk-In Interview for Quality Assurance (IPQA) Roles – July 2, 2025

BDR Pharmaceuticals International Pvt. Ltd., a leading pharmaceutical company established in 2002, is hosting a walk-in interview for Quality Assurance (IPQA) roles at our Baska, Gujarat facility. Renowned for API and formulation manufacturing in oncology, critical care, gynecology, and neurology, BDR operates USFDA, WHO-GMP, and EU-GMP compliant plants.

Certified as a Great Place to Work (Jan 2024–Jan 2025), we are committed to making healthcare affordable and accessible. Join our team at the Baska plant to be a part of change-makers and make an impact in pharmaceutical quality assurance!

Walk-In Interview Details

• Date: Wednesday, July 2, 2025
• Time: 9:00 AM to 5:00 PM
• Venue & Job Location: BDR Pharmaceuticals International Pvt. Ltd., Survey No. 51/1/2, 52/1/2, Vanseti Village, PO-Tajpura, TA-Halol, District: Baska, Gujarat – 389350

Contact:

• Darpan Rajput: +91 9998324795, darpan.rajput@bdrpharma.com
• Divya Jadav: +91 7778054628, divya.jadav@bdrpharma.com
• Neha Thakkar: +91 6358139082, neha.thakkar@bdrpharma.com

Required Documents:

• Updated resume (2 copies)
• Original and photocopies of educational certificates (B.Pharm/M.Pharm/M.Sc)
• Last 3 months’ payslips and latest increment letter
• Aadhar card and PAN card
• Passport-size photographs (2)

Note:

• Candidates must have experience in regulated plants (e.g., USFDA, EU-GMP).
• Candidates interviewed at BDR in the last 6 months are ineligible.
• This walk-in is exclusively for the listed QA (IPQA) roles. For other roles, visit BDR Careers.

Open Positions – Quality Assurance (IPQA)

IPQA (General Injection Manufacturing)

Officer

• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 4–6 years
• Responsibilities: Conduct in-process quality checks, line clearance, and sampling for general injectable manufacturing; review BMR/BPR; manage deviations and CAPA.
• Key Skills: Knowledge of cGMP, GDP, and aseptic practices in sterile injectables.

Senior Officer

• Qualification: B.Pharm / M.Pharm / M.Sc
• Experience: 4–6 years
• Responsibilities: Oversee IPQA activities, ensure compliance with SOPs, and support USFDA/MHRA audits for injectable production.
• Key Skills: Strong regulatory knowledge and experience in sterile manufacturing.

Executive

• Qualification: B.Pharm / M.Pharm
• Experience: 5–7 years
• Responsibilities: Manage IPQA for general injectables, handle QMS, deviations, OOS, and audit compliance.
• Key Skills: Expertise in QMS, regulatory audits, and injectable processes.

Senior Executive

• Qualification: B.Pharm / M.Pharm
• Experience: 7–10 years
• Responsibilities: Lead IPQA operations, ensure regulatory compliance, and mentor junior staff in injectable manufacturing.
• Key Skills: Leadership in QA processes and regulatory expertise.

Quality Assurance (Process and Cleaning Validation, Equipment Validation – OSD, APQR, QMS – General Injectable)

Executive

• Qualification: B.Pharm / M.Pharm
• Experience: 5–7 years
• Key Skills: Expertise in validation protocols, QMS, and regulatory compliance (USFDA, EU-GMP).

Responsibilities:

• Conduct process and cleaning validation for general injectable manufacturing.
• Perform equipment validation for Oral Solid Dosage (OSD).
• Prepare Annual Product Quality Review (APQR) reports.
• Manage Quality Management System (QMS) activities, including change control and deviations.

Why Join BDR Pharmaceuticals?

• Global Impact: Contribute to a company with a strong presence in oncology and critical care, exporting to 60+ countries with USFDA and EU-GMP compliant facilities.
• Great Place to Work: Rated 4.2/5 on AmbitionBox for job security and supportive culture, with a robust induction program and HR support.
• State-of-the-Art Facility: Work in Baska’s advanced plant, specializing in general injectables and equipped with isolators and solvent recovery systems.
• Career Growth: Benefit from a talent-focused environment, though long working hours and limited parental mediclaim coverage are noted drawbacks.

How to Apply

• Walk-In: Attend the interview on July 2, 2025, at BDR Pharmaceuticals, Baska, with all required documents.
• For Those Unable to Attend: Email your updated CV to darpan.rajput@bdrpharma.com, divya.jadav@bdrpharma.com, or neha.thakkar@bdrpharma.com, mentioning the specific role (e.g., “IPQA Officer – General Injection”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.

Note: Candidates with USFDA-approved plant experience in general injectables or OSD are preferred.

About BDR Pharmaceuticals

Established in 2002, BDR Pharmaceuticals International Pvt. Ltd. is a Mumbai-based leader in API and formulation manufacturing, focusing on oncology, critical care, gynecology, and neurology. With facilities in Vadodara (Baska, Luna), Surat, and Hyderabad, BDR ensures affordable, high-quality medicines through multi-branding strategies.

The Baska plant, specializing in general injectables, is USFDA, WHO-GMP, and EU-GMP compliant, with plans for ANVISA audits. Employing over 1,000 professionals, BDR fosters innovation and career growth in a supportive environment. Learn more at www.bdrpharma.com.

Important Disclaimer

BDR Pharmaceuticals does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers to Ombudsman@bdrpharma.com or call +91-22-40560560.

Join BDR Pharmaceuticals at our Baska plant and be a change-maker in quality healthcare!