Centaur Pharmaceuticals Pvt. Ltd., one of India’s rapidly growing pharmaceutical companies, is hosting a walk-in interview at our USFDA and MHRA-approved Oral Solid Dosage (OSD) manufacturing facility in Pune. Renowned for delivering high-quality, affordable medicines trusted globally, we are seeking experienced professionals to join our Analytical R&D, Quality Control, Quality Assurance, and HR & Admin teams.
If you have expertise in formulations and regulatory audits, this is your chance to contribute to a leading organization committed to excellence in the pharmaceutical industry.
Walk-In Interview Details
- Date: Sunday, May 4, 2025
- Time: 9:30 AM to 4:00 PM
- Venue: Centaur Pharmaceuticals Pvt. Ltd., Plot No. 4, International Biotech Park, Hinjewadi Phase II, Pune, Maharashtra 411057
- Contact: +91-20-66739478
- Email: hrpune@centaur.co.in
Job Description
We are hiring experienced candidates with a strong background in formulations and exposure to regulatory audits (USFDA, MHRA, EU) for our Pune facility. Below are the details of the open positions:
Analytical R&D
Position: Research Associate / Senior Research Associate
- Experience: 2-6 years
- Qualifications: M.Sc.
- Responsibilities: Conduct analytical method development, validation, and testing for OSD formulations, ensuring compliance with regulatory standards.
Quality Control
Position: Officer / Executive / Senior Executive
- Experience: 4-10 years
- Qualifications: B.Sc. / M.Sc. (Chemistry)
- Sections: Raw Material (RM), In-Process & Finished Product (FP), Stability, Analytical Method Validation (AMV), Analytical Method Transfer (AMT), Good Laboratory Practices (GLP), Quality Management System (QMS), Packaging Material (PM)
- Responsibilities: Perform analysis of raw materials, in-process, and finished products; handle stability testing, AMV/AMT, and sophisticated instruments like HPLC and dissolution testers.
Position: Senior Executive / Assistant Manager
- Experience: 10-15 years
- Qualifications: B.Pharm / M.Pharm / M.Sc.
- Sections: Finished Product (FP), In-Process (IP), Stability, GLP
- Responsibilities: Oversee QC operations, ensure compliance with GLP, and manage stability studies and regulatory audits.
Quality Assurance
Position: Officer / Executive
- Experience: 4-10 years
- Qualifications: B.Pharm / M.Pharm / M.Sc.
- Sections: Quality Management System (QMS), Analytical Quality Assurance (AQA), In-Process Quality Assurance (IPQA), IT (QA), Validation, Documentation
- Responsibilities: Manage QMS elements (deviation, CAPA, change control), conduct validations, and ensure compliance with cGMP and regulatory requirements.
Position: Assistant Manager
- Experience: 10-15 years
- Qualifications: M.Pharm / M.Sc.
- Section: Analytical Quality Assurance (AQA)
- Responsibilities: Lead AQA activities, review analytical data, and ensure audit readiness for USFDA, MHRA, and EU inspections.
HR & Admin
Position: Executive / Senior Executive
- Experience: 7-11 years
- Qualifications: MBA (HRM)
- Preferences: Male candidates with pharmaceutical industry experience
- Responsibilities: Handle recruitment, employee relations, compliance with labor laws, and administrative tasks in a regulated pharma environment.
Additional Requirements
- Candidates must have experience in formulations at a regulated manufacturing company (USFDA, MHRA, EU).
- Exposure to regulatory audits (USFDA, MHRA, EU) is mandatory.
- Willingness to work in shifts as required.
How to Apply
Interested candidates should attend the walk-in interview on May 4, 2025, at the specified venue with:
- A detailed resume
- A recent passport-size photograph
- Relevant educational and experience certificates
Candidates unable to attend can email their resume to hrpune@centaur.co.in or contact +91-20-66739478 for further details. Shortlisted candidates will be contacted for the next steps in the recruitment process.
Why Choose Centaur Pharmaceuticals?
Centaur Pharmaceuticals, headquartered in Mumbai, is a vertically integrated pharmaceutical company with a global presence in 96 countries and 42% of sales from international markets. Our USFDA and MHRA-approved Pune facility specializes in OSD manufacturing for regulatory markets, offering a collaborative and innovative work environment.
Rated 3.5/5 on AmbitionBox based on 501 employee reviews, we provide competitive salaries, comprehensive benefits, and opportunities for professional growth. Join us to contribute to high-quality pharmaceutical solutions while advancing your career in a rapidly growing organization trusted by healthcare professionals worldwide.