Centaur Pharmaceuticals Pvt. Ltd. has announced a walk-in interview for experienced professionals in the Quality Assurance (QA) and Quality Control (QC) departments at its Hinjewadi facility in Pune, Maharashtra.

Candidates with relevant pharmaceutical industry experience and knowledge of regulatory compliance, quality systems, analytical testing, validation, and laboratory operations can apply for the available positions.

Walk-In Interview Details

Company Name: Centaur Pharmaceuticals Pvt. Ltd.

Interview Date: 1 November 2026

Interview Time: 8:30 AM onwards

Job Location: Hinjewadi, Pune, Maharashtra

Venue: Plot No. 4, International Biotech Park, Hinjewadi Phase II, Pune, Maharashtra – 411057

Email ID: hrpune@centaur.co.in

Contact Number: +91-20-66739510

1. Quality Assurance (QA) Vacancies

1. Executive / Senior Executive – ITQA Qualification: B.Pharm / M.Pharm / M.Sc. Experience: 6–10 years
2. Assistant Manager / Deputy Manager – QMS Investigations Qualification: B.Pharm / M.Pharm / M.Sc. Experience: 12–16 years
3. Assistant Manager / Deputy Manager – Analytical QA Qualification: B.Pharm / M.Pharm / M.Sc. Experience: 12–16 years
4. Senior Officer / Executive – Qualification / Validation Qualification: B.Pharm / M.Pharm Experience: 5–10 years

2. Quality Control (QC) Vacancies

1. Assistant Manager / Deputy Manager – RM Section Head Qualification: M.Sc. Experience: 12–16 years
2. Assistant Manager / Deputy Manager – Stability Section Head Qualification: M.Sc. Experience: 12–16 years
3. Assistant Manager / Deputy Manager – AMV/AMT Section Head Qualification: M.Sc. Experience: 12–16 years
4. Assistant Manager / Deputy Manager – GLP Section Head Qualification: M.Sc. Experience: 12–16 years
5. Executive / Senior Executive – QMS Qualification: M.Sc. Experience: 10–15 years
6. Officer / Senior Officer – HPLC, GC, UV, Dissolution and Other Sophisticated Instruments Qualification: M.Sc. Experience: 3–5 years
7. Junior Executive / Executive – HPLC, GC, UV, Dissolution and Other Sophisticated Instruments Qualification: M.Sc. Experience: 6–10 years
8. Officer / Senior Officer – LIMS Master and Specification Preparation Qualification: M.Sc. Experience: 3–5 years
9. Junior Executive / Executive – LIMS Master and Specification Review Qualification: M.Sc. Experience: 8–12 years

Eligibility Criteria

Candidates should have experience in pharmaceutical formulation manufacturing, particularly in regulated markets such as the USFDA, MHRA, and EU.

Experience with regulatory audits is mandatory as mentioned in the recruitment advertisement. Candidates should have the relevant qualifications, technical knowledge, and experience required for their preferred position.

How to Apply

Interested candidates can attend the walk-in interview directly at the venue mentioned above.

Candidates who cannot attend the interview can send their updated resume and a recent passport-size photograph to:

Email: hrpune@centaur.co.in

Contact: +91-20-66739510

Candidates should carry their updated resume, educational certificates, experience certificates, photographs, and valid photo ID.

Technical FAQs

1. What is ITQA in the pharmaceutical industry?

ITQA means Information Technology Quality Assurance. It involves ensuring that computerized systems used in pharmaceutical operations meet applicable quality and regulatory requirements.

2. What is QMS in pharmaceutical manufacturing?

QMS stands for Quality Management System. It includes procedures for deviations, investigations, CAPA, change control, documentation, and continuous improvement.

3. What is analytical method validation?

Analytical method validation demonstrates that an analytical procedure is suitable for its intended purpose. It may include testing parameters such as accuracy, precision, specificity, linearity, and range.

4. What is stability testing in pharmaceuticals?

Stability testing evaluates how the quality of a drug substance or finished product changes over time under specified environmental conditions. It helps establish shelf life and storage requirements.

5. What is the role of HPLC, GC, and LIMS in pharmaceutical quality control?

HPLC and GC are analytical techniques used to test pharmaceutical materials and products. LIMS stands for Laboratory Information Management System and supports laboratory data management, sample tracking, documentation, and reporting.

Important Note

The above recruitment information is based on the supplied advertisement. Candidates should confirm the interview schedule and vacancy details with Centaur Pharmaceuticals before travelling or applying.