Centaur Pharma Walk-In Interview For QA,QC & Production Departments || 9 November 2025

Centaur Pharma Walk-In Interview For QA,QC & Production Departments || 9 November 2025

Walk-In Interview – Centaur Pharmaceuticals Pvt. Ltd.

Walk-In Interview Details:

Date: 09 November 2025 (Sunday)

Time: 09:00 AM to 04:00 PM

Venue: Centaur Pharmaceuticals Pvt. Ltd., Plot No. 4, International Biotech Park, Hinjewadi Phase II, Pune – 411057

Centaur Pharmaceuticals is hiring experienced professionals for its QA and QC departments at the Pune facility. If you have relevant experience in formulation manufacturing and regulatory audits, join India’s fastest-growing research-driven pharmaceutical organization.

Open Positions:

A.Quality Control Department

1.Officer / Sr. Officer

  • Sections: RM & PM, In-Process & FP, Stability, AMV & AMT, GLP & QMS, Microbiology
  • Experience: 4–8 Years
  • Qualification: M.Sc / B.Pharm / M.Pharm

2.Executive / Sr. Executive

  • Sections: RM & PM, In-Process & FP, Stability, AMV & AMT, GLP & QMS, Microbiology
  • Experience: 8–12 Years
  • Qualification: M.Sc / B.Pharm / M.Pharm

3.Asst. Manager (Section Head)

  • Sections: Raw Material, GLP, Stability, AMV & AMT
  • Experience: 12–16 Years
  • Qualification: M.Sc / B.Pharm / M.Pharm

B.Quality Assurance Department


1.Sr. Officer / Executive / Sr. Executive

  • Sections: Analytical QA, Validation, In-Process QA, CSV-QA
  • Experience: 4–10 Years
  • Qualification: B.Pharm / M.Pharm / M.Sc

C.Production Department


1.Trainee Operator

  • Sections: Granulation, Compression, Coating, Packing
  • Experience: Fresher
  • Qualification: B.Sc / D.Pharm / ITI
Candidate Requirements:
  • Experience in formulation regulatory manufacturing (USFDA, MHRA, EU)
  • Exposure to regulatory audits is mandatory

How to Apply: Send your cv at  📧 Email: hrdesk.pune@centaur.co.in 

 Bring: Detailed resume and recent passport-size photograph

Centaur Pharma Walk-In Interview For QA,QC & Production Departments || 9 November 2025
Centaur Pharma Walk-In Interview For QA,QC & Production Departments || 9 November 2025

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