BDR Pharmaceuticals Walk-in Drive for QC, Production, ADL, R&D, and Analytical QA

BDR Pharmaceuticals, a trusted name in the pharmaceutical industry, is conducting a walk-in drive to recruit talented professionals for multiple roles in Quality Control (QC), Production, ADL, R&D, and Analytical QA. This is a golden opportunity for candidates with relevant qualifications and experience to join a company recognized as a “Great Place to Work.”

Walk-in Interview Details

• Date: 19th January 2025 (Sunday)
• Time: 10:00 AM to 5:00 PM
• Venue:
  R.S No. 578, Near Effluent Channel Road,
  Vill. Luna, Tal. Padra,
  Dist. Vadodara, Gujarat – 391440

Available Roles and Eligibility Criteria

1. Quality Control (Formulation)
   • Designation: Officer to Senior Executive
   • Qualification: B.Sc or M.Sc
   • Experience: 2 to 8 years
   • Responsibilities:
     • Conduct quality analysis of raw materials, intermediates, and finished products.
     • Ensure compliance with regulatory guidelines.
     • Maintain and review quality control documentation.
2. Production (ONCO – OSD)
   • Designation: Technician to Assistant Manager
   • Qualification: ITI, B.Pharm, or M.Pharm
   • Experience: 2 to 12 years
   • Responsibilities:
     • Oversee production processes in the oncology oral solid dosage (OSD) unit.
     • Ensure adherence to GMP and safety standards.
     • Handle equipment and manage production schedules.
3. ADL & CVC (API & Formulation)
   • Designation: Officer to Senior Officer
   • Qualification: M.Sc
   • Experience: 2 to 4 years
   • Responsibilities:
     • Develop and validate analytical methods for API and formulations.
     • Conduct stability studies and compile analytical reports.
     • Ensure compliance with regulatory standards.
4. R&D (API Synthesis)
   • Designation: Officer to Senior Executive
   • Qualification: M.Sc
   • Experience: 2 to 8 years
   • Responsibilities:
     • Perform API synthesis and process development.
     • Optimize synthetic routes for cost-effectiveness and scalability.
     • Document R&D activities and ensure regulatory compliance.
5. Analytical QA (Formulation)
   • Designation: Executive to Senior Executive
   • Qualification: M.Sc or M.Pharm
   • Experience: 4 to 8 years
   • Responsibilities:
     • Ensure analytical QA processes align with regulatory requirements.
     • Review analytical data and reports.
     • Support audits and inspections by regulatory bodies.

Application Process

• Walk-in: Attend the interview at the venue on the specified date and time.
• Documents to Carry:
  • Updated resume
  • Aadhar card
  • 3 months’ pay slips
  • Current CTC letter
• Email for Queries: Send your resume to kunal.karachiwala@bdrpharma.com