Centaur Pharmaceuticals Pvt. Ltd. has announced a Walk-in Interview for experienced professionals and freshers at its Pune manufacturing facility. The company is hiring candidates for Quality Control (QC), Quality Assurance (QA), Production, Engineering, Purchase, and DQA departments. Candidates with experience in OSD (Oral Solid Dosage) formulation manufacturing and exposure to USFDA, MHRA, and EU regulatory requirements are encouraged to attend.

Job Overview

Particular Details

Company Name

Centaur Pharmaceuticals Pvt. Ltd.

Job Type

Walk-in Interview

Interview Date

26 July 2026

Time

8:30 AM Onwards

Job Location

Hinjewadi Phase-II, International Biotech Park, Pune, Maharashtra

Industry

Pharmaceutical (OSD Formulation)

Department-wise Vacancy Details

1. Quality Control (QC)

Officer / Sr. Officer / Jr. Executive

Role: Handling HPLC, GC, UV, Dissolution and other sophisticated analytical instruments

Qualification: M.Sc.

Experience: 3–9 Years

Executive / Sr. Executive

Role:

OOS

OOT

CAPA

Change Control

Audit Compliance

Qualification: M.Sc.

Experience: 6–10 Years

Assistant Manager / Deputy Manager

Role:

Stability

AMV

AMT

GLP

Reference Material Management

Qualification: M.Sc.

Experience: 12–16 Years

2. Quality Assurance (QA)

Executive / Sr. Executive

Investigation Lead

Audit & Compliance

Documentation Cell

Qualification

B.Pharm

M.Pharm

M.Sc.

Experience

6–10 Years

Assistant Manager / Deputy Manager

Responsibilities

QMS

AQA

Plant Regulatory Affairs

TTQA

Qualification

B.Pharm

M.Pharm

M.Sc.

Experience

12–16 Years

3. Production Department

Officer / Sr. Officer

Responsibilities

Granulation

Compression

Coating

Packing Supervision

Qualification

B.Sc.

B.Pharm

Experience

2–5 Years

Executive / Sr. Executive (Shift In-charge)

Responsibilities

Overall Production Shift Activities

Qualification

B.Pharm

M.Pharm

Experience

10–14 Years

Operator / Sr. Operator

Responsibilities

Granulation

Compression

Coating

Blister Packing

Qualification

H.Sc.

D.Pharm

B.Sc.

Experience

2–5 Years

Trainee Operator

Department

Production

Qualification

D.Pharm

B.Sc.

ITI

Experience

Freshers Eligible

4. Engineering Department

Officer / Executive

Process Maintenance

Qualification: DME / BE

Experience: 4–8 Years

Officer

ETP/STP Operations

Qualification: B.Sc. / Chemical Engineering

Experience: 3–4 Years

Fitter / Electrician

Plant Maintenance

Qualification: ITI / DME

Experience: 4–6 Years

Important Eligibility Criteria

Candidates should have:

Experience in Regulatory OSD Formulation Manufacturing

Exposure to USFDA, MHRA, and EU regulatory audits

Knowledge of GMP documentation and pharmaceutical compliance

Relevant qualification and experience as mentioned for the respective position

Candidates Unable to Attend

Candidates who cannot attend the walk-in interview may send their updated resume to:

hrpune@centaur.co.in

hrdesk_pune@centaur.co.in

Additionally, Purchase and DQA department candidates can directly share their resume with:

hrdesk_pune@centaur.co.in

Walk-in Venue

Centaur Pharmaceuticals Pvt. Ltd.

Hinjewadi Phase-II, International Biotech Park, Pune, Maharashtra

Interview Date: 26 July 2026

Reporting Time: 8:30 AM Onwards

Documents to Carry

Updated Resume

Passport-size Photographs

Educational Certificates

Experience Certificates

Latest Salary Slips

PAN Card

Aadhaar Card

Government Photo ID

Why Join Centaur Pharmaceuticals?

Opportunity to work with a reputed pharmaceutical manufacturer

Exposure to international regulatory standards

Career growth in QA, QC, Production and Engineering

Modern manufacturing facilities

Learning opportunities in GMP, QMS and regulatory compliance

Technical FAQs

1. What analytical instruments should QC candidates be proficient in?

Candidates should have practical experience with HPLC, GC, UV-Visible Spectrophotometer, Dissolution Test Apparatus, and other analytical laboratory instruments used in pharmaceutical quality control.

2. What is OOS and OOT in pharmaceutical quality systems?

OOS (Out of Specification) refers to test results outside approved specifications, while OOT (Out of Trend) refers to results that deviate from historical trends. Both require documented investigation under GMP.

3. What is CAPA in pharmaceutical manufacturing?

CAPA (Corrective and Preventive Action) is a quality management process used to investigate deviations, identify root causes, implement corrective actions, and prevent recurrence to ensure regulatory compliance.

4. Why is USFDA, MHRA, and EU audit exposure important?

Experience with these regulatory agencies demonstrates familiarity with global GMP standards, documentation practices, data integrity requirements, and inspection readiness expected in regulated pharmaceutical manufacturing.

5. What are the responsibilities of Production Shift In-charge in an OSD plant?

A Production Shift In-charge manages manufacturing operations, manpower allocation, batch execution, equipment utilization, GMP compliance, production documentation, safety, and coordination with QA, QC, and Engineering teams.