Centaur Pharmaceuticals is conducting a walk-in drive on 24th May 2026 in Pune for multiple pharma jobs in Quality Control, Quality Assurance, Production, and Engineering. Excellent opportunity for experienced professionals seeking pharmaceutical careers in India in regulated OSD manufacturing.
Contents
- 1 About the Company
- 2 Job Details
- 3 Job Description
- 3.1 Quality Control Officer / Sr. Officer
- 3.2 Quality Control – Microbiology Officer/Executive
- 3.3 Asst. Manager / Dy. Manager – Quality Control (Stability / AMV)
- 3.4 Production Officer / Sr. Officer
- 3.5 Production Operator / Sr. Operator
- 3.6 Quality Assurance Executive / Sr. Executive
- 3.7 Quality Assurance Asst. Manager / Dy. Manager
- 3.8 Engineering Officer / Executive (Process Maintenance)
- 3.9 Engineering Operator / Fitter / Electrician
- 4 Skills/Qualifications
- 5 Key Responsibilities
- 6 Benefits/Perks
- 7 How to Apply
- 8 Walk-in Interview Details
- 9 Why You Should Join
- 10 FAQs
About the Company
Centaur Pharmaceuticals Pvt. Ltd. is a well-established Indian pharmaceutical company known for its high-quality formulations and strong regulatory compliance. With a focus on innovation and quality healthcare solutions, Centaur operates modern manufacturing facilities in Pune and Goa. The company has a successful track record of meeting stringent international standards including USFDA, MHRA, and EU-GMP, serving both domestic and global markets.
Its commitment to excellence makes it a preferred employer for professionals looking for stable growth in the pharma industry.
Job Details
- Company Name: Centaur Pharmaceuticals Pvt. Ltd.
- Experience: 2 to 16 Years (varies by role)
- Qualification: B.Sc / M.Sc / B.Pharma / M.Pharma / Diploma / ITI / BE / DME
- Location: Pune & Goa
- Work Type: On-site
Job Description
Centaur Pharmaceuticals is hiring experienced talent for its regulatory OSD formulation facilities in Pune and Goa. This walk-in interview covers multiple roles in Quality Control, Quality Assurance, Production, and Engineering departments. Candidates with exposure to USFDA, MHRA, and EU audits are encouraged to apply.
Quality Control Officer / Sr. Officer
- Department: Quality Control
- Experience: 3 to 8 Years (Pune) / 3 to 10 Years
- Education/Qualification: M.Sc
Quality Control – Microbiology Officer/Executive
- Department: Quality Control
- Experience: 3 to 6 Years
- Education/Qualification: M.Sc (Microbiology)
Asst. Manager / Dy. Manager – Quality Control (Stability / AMV)
- Department: Quality Control
- Experience: 12 to 16 Years
- Education/Qualification: M.Sc
Production Officer / Sr. Officer
- Department: Production
- Experience: 4 to 7 Years (Goa) / 2 to 5 Years
- Education/Qualification: B.Sc / B.Pharma / M.Pharma
Production Operator / Sr. Operator
- Department: Production
- Experience: 3 to 7 Years
- Education/Qualification: Diploma / Graduate (experienced)
Quality Assurance Executive / Sr. Executive
- Department: Quality Assurance
- Experience: 6 to 10 Years
- Education/Qualification: B.Pharma / M.Pharma / M.Sc
Quality Assurance Asst. Manager / Dy. Manager
- Department: Quality Assurance
- Experience: 12 to 16 Years
- Education/Qualification: B.Pharma / M.Pharma / M.Sc
Engineering Officer / Executive (Process Maintenance)
- Department: Engineering
- Experience: 4 to 8 Years
- Education/Qualification: BE / Diploma / DME
Engineering Operator / Fitter / Electrician
- Department: Engineering
- Experience: 4 to 6 Years
- Education/Qualification: ITI / DME
Skills/Qualifications
- Hands-on experience in HPLC, GC, UV, Dissolution, and Caliber LIMS
- Strong knowledge of Process Validation, AQA, IPQA, QMS, and Documentation
- Experience in Granulation, Compression, Coating, and Packing operations
- Exposure to USFDA, MHRA, and EU regulatory audits (mandatory)
- Equipment maintenance and water system handling skills
- Excellent teamwork and compliance-oriented approach
Key Responsibilities
- Perform HPLC, GC, UV, and Dissolution testing
- Handle stability studies and analytical method validation
- Supervise granulation, compression, coating, and packing
- Conduct process validation and audit compliance activities
- Maintain QMS documents and support regulatory audits
- Perform plant maintenance and engineering operations
Benefits/Perks
- Career growth in a regulated OSD manufacturing environment
- Opportunities for skill development and cross-functional exposure
- Competitive salary and performance–based benefits
- Professional work culture with focus on quality
- Global regulatory exposure and learning opportunities
How to Apply
Candidates should walk in with a detailed resume and recent passport-size photograph. Those unable to attend can email their resume.
Pune: hrpune@centaur.co.in Goa: tuem_hr@centaurgoa.com
For more pharma jobs across India, visit Pharma Recruiter.
Apply now and grow your career with Centaur Pharmaceuticals!
Walk-in Interview Details
- Date: 24th May 2026 (Sunday)
- Time: 8:30 AM onwards
- Venue: Centaur Pharmaceuticals Pvt. Ltd., Plot No-4, Phase-II, International Biotech Park, Hinjewadi, Pune-411057
- Contact/Email: Walk-in preferred | hrpune@centaur.co.in
Why You Should Join
Centaur Pharmaceuticals values innovation, compliance, and employee growth in a collaborative environment. Joining the team offers long-term career stability, recognition for performance, and excellent opportunities to work with advanced technologies while contributing to quality healthcare solutions in a globally compliant setting.
FAQs
Q1: What experience is required?
Experience ranges from 2–16 years depending on the position. Regulatory OSD formulation background is preferred.
Q2: Which locations are available?
Positions are open at Pune and Goa manufacturing facilities.
Q3: Is prior regulatory audit exposure mandatory?
Yes, experience with USFDA, MHRA, and EU audits is mandatory for most roles.
Q4: Can candidates who cannot attend walk-in apply?
Yes, they can email their resume to hrpune@centaur.co.in (Pune) or tuem_hr@centaurgoa.com (Goa).
