Centaur Pharmaceuticals is inviting applications from experienced professionals for multiple Quality Assurance (QA) and Quality Control (QC) positions at its facility in Hinjewadi, Pune, Maharashtra. The vacancies are intended for candidates with pharmaceutical manufacturing experience, strong GMP knowledge, and exposure to regulatory requirements in regulated formulation manufacturing environments.
The recruitment includes opportunities for QC Analysts, QC Section Heads, and experienced QA professionals in Technology Transfer Development, Quality Management Systems (QMS), and Analytical Quality Assurance (AQA). Candidates with relevant experience in regulatory pharmaceutical manufacturing and exposure to USFDA, MHRA, and European regulatory audits may be suitable for these positions.
Centaur Pharmaceuticals Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Centaur Pharmaceuticals |
| Job Category | Pharmaceutical QA and QC Jobs |
| Job Location | Hinjewadi, Phase II, Pune, Maharashtra |
| QC Qualification | M.Sc |
| QA Qualification | B.Pharm, M.Pharm or M.Sc, depending on the position |
| Experience Required | 4–16 years, depending on the role |
| Industry | Pharmaceutical Formulation Manufacturing |
| Salary | Not specified in the available vacancy details |
| Application Mode | |
| Contact Email | hrpune@centaur.co.in |
| Contact Number | 020-66739510 |
1. Centaur Pharmaceuticals Quality Control (QC) Vacancies
Centaur Pharmaceuticals has openings across several Quality Control functions, including stability studies, Analytical Method Validation (AMV), Analytical Method Transfer (AMT), raw materials (RM), Good Laboratory Practices (GLP), and routine QC analysis.
QC Positions and Eligibility
| Position | Department/Section | Qualification | Experience |
|---|---|---|---|
| Assistant Manager / Deputy Manager | Stability – Section Head | M.Sc | 12–16 years |
| Assistant Manager / Deputy Manager | AMV / AMT – Section Head | M.Sc | 12–16 years |
| Assistant Manager / Deputy Manager | Raw Materials (RM) – Section Head | M.Sc | 12–16 years |
| Assistant Manager / Deputy Manager | GLP – Section Head | M.Sc | 12–16 years |
| Officer / Senior Officer | QC Analyst | M.Sc | 4–6 years |
QC Job Responsibilities
Depending on the assigned section and designation, selected candidates may be responsible for:
- Managing day-to-day Quality Control activities in the assigned laboratory or section.
- Following approved procedures and maintaining GMP-compliant laboratory practices.
- Ensuring accurate documentation and adherence to applicable quality standards.
- Supporting laboratory readiness for regulatory inspections and customer audits.
- Performing or overseeing activities related to stability studies, analytical method validation and transfer, raw material testing, GLP, or QC analysis.
- Maintaining a strong focus on data accuracy, documentation quality, and compliance.
QC Eligibility Requirements
Applicants should have an M.Sc qualification and relevant experience in pharmaceutical Quality Control. Section Head positions require approximately 12–16 years of experience, while the QC Analyst opening requires 4–6 years.
Experience in regulated formulation manufacturing environments and familiarity with inspections or audits involving USFDA, MHRA, and European regulatory requirements are important considerations.
2. Centaur Pharmaceuticals Quality Assurance (QA) Vacancies
The Quality Assurance department is recruiting experienced professionals for Technology Transfer Development, Quality Management Systems, and Analytical Quality Assurance.
QA Positions and Eligibility
| Position | Functional Area | Qualification | Experience |
|---|---|---|---|
| Executive / Senior Executive | Technology Transfer Development | B.Pharm / M.Pharm | 8–12 years |
| Assistant Manager / Deputy Manager | Quality Management Systems (QMS) | B.Pharm / M.Pharm / M.Sc | 12–16 years |
| Assistant Manager / Deputy Manager | Analytical Quality Assurance (AQA) | B.Pharm / M.Pharm / M.Sc | 12–16 years |
QA Job Responsibilities
Responsibilities will depend on the selected function and level of the position. Typical duties may include:
- Supporting the implementation and maintenance of pharmaceutical quality systems.
- Coordinating quality activities associated with technology transfer and product development.
- Supporting Analytical Quality Assurance activities and relevant laboratory quality processes.
- Maintaining documentation and ensuring compliance with applicable GMP requirements.
- Assisting with regulatory audit preparedness and follow-up activities.
- Coordinating with relevant departments to support quality objectives and continuous improvement.
QA Eligibility Requirements
Candidates should possess the qualification specified for their preferred position and have the relevant pharmaceutical industry experience.
For Technology Transfer Development, B.Pharm or M.Pharm candidates with 8–12 years of experience are invited to apply. QMS and AQA positions are intended for candidates with B.Pharm, M.Pharm, or M.Sc qualifications and 12–16 years of relevant experience.
Exposure to regulated formulation manufacturing and regulatory inspections involving USFDA, MHRA, or European requirements is desirable based on the vacancy description.
Skills Required for Centaur Pharmaceuticals QA and QC Jobs
Candidates applying for these positions should have relevant functional experience and a strong understanding of pharmaceutical quality requirements. Depending on the role, useful competencies include:
- Good Manufacturing Practices (GMP).
- Pharmaceutical quality systems and compliance documentation.
- Regulatory inspection and audit preparedness.
- Quality Control laboratory operations.
- Stability studies and analytical method validation or transfer.
- Raw material testing and GLP practices.
- Technology transfer and Analytical Quality Assurance.
- Documentation accuracy, coordination, and attention to detail.
The specific technical requirements may differ between section-level, officer-level, and management positions.
Job Location
The vacancies are based at:
Centaur Pharmaceuticals
Hinjewadi, Phase II, International Biotech Park, Pune, Maharashtra, India.
Candidates should confirm the exact work location and reporting arrangements with the recruitment team before joining.
Salary and Benefits
The salary package and benefits have not been specified in the available vacancy announcement. Compensation may depend on the designation, relevant experience, qualifications, and the company’s recruitment terms.
Candidates can contact the HR team for information about compensation, benefits, working hours, and other employment conditions.
How to Apply for Centaur Pharmaceuticals Recruitment 2026
Eligible candidates can apply by sending their updated resume and a recent passport-size photograph to the recruitment email address provided below.
Email: hrpune@centaur.co.in
Contact Number: 020-66739510
Applicants should mention their preferred position, relevant department, and total years of pharmaceutical industry experience in the email subject or message. They should also highlight their experience in regulated formulation manufacturing and relevant regulatory audits, where applicable.
Before sending an application, candidates should verify the vacancy details and confirm that their qualifications and experience match the requirements of the selected position.
Frequently Asked Questions (FAQs)
1. Which company is recruiting for QA and QC jobs in Pune?
Centaur Pharmaceuticals is inviting applications for experienced Quality Assurance and Quality Control professionals at its Hinjewadi facility in Pune.
2. Which QC positions are available?
The listed QC openings include Section Head roles in Stability, AMV/AMT, Raw Materials, and GLP, along with Officer/Senior Officer positions for QC Analysts.
3. What qualifications are required for QC jobs?
An M.Sc qualification is specified for the listed QC positions.
4. How much experience is required for QC vacancies?
The QC Analyst position requires 4–6 years of experience, while the listed QC Section Head positions require 12–16 years.
5. Which QA positions are available?
The QA vacancies include Executive/Senior Executive – Technology Transfer Development, Assistant Manager/Deputy Manager – QMS, and Assistant Manager/Deputy Manager – AQA.
6. What qualifications are required for QA jobs?
Technology Transfer Development requires B.Pharm or M.Pharm. QMS and AQA positions accept B.Pharm, M.Pharm, or M.Sc, as specified in the vacancy details.
7. How much experience is needed for QA positions?
Technology Transfer Development requires 8–12 years, while QMS and AQA positions require 12–16 years of experience.
8. Where are these vacancies located?
The positions are based in Hinjewadi, Phase II, International Biotech Park, Pune, Maharashtra.
9. How can candidates apply?
Candidates can email their updated resume and recent passport-size photograph to hrpune@centaur.co.in.
10. Is the salary mentioned in the vacancy?
No. The available vacancy information does not specify a salary package.
Important Disclaimer
This article is a rewritten summary of a third-party vacancy listing and is not an official recruitment notification from Centaur Pharmaceuticals. Job availability, eligibility requirements, experience criteria, salary, and application procedures may change. Candidates should confirm the latest information with the company’s recruitment team before applying.