Discover exciting pharma jobs in Quality Assurance at Centaur Pharmaceuticals. This is a great opportunity for experienced professionals seeking QA jobs in a regulated OSD manufacturing environment with strong exposure to USFDA, MHRA, and EU audits. Explore pharmaceutical careers in India with a leading player in the industry.
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About the Company
Centaur Pharmaceuticals Pvt. Ltd. is one of India’s few fully integrated pharmaceutical companies with expertise across the entire value chain, including API, formulations, R&D, contract research, and clinical research.
Established in 1978, the company ranks among India’s top pharmaceutical firms by prescriptions and maintains a strong presence across Asia, South America, and Africa, exporting to over 120 countries.
With a strong focus on innovation, quality, and regulatory compliance, Centaur leverages advanced manufacturing facilities and strategic global alliances to deliver high-quality pharmaceutical solutions.
The company is committed to continuous growth, operational excellence, and “We Impart Health to Life” philosophy, making it an ideal destination for professionals passionate about pharmaceutical careers in India.
Job Details
- Company Name: Centaur Pharmaceuticals Pvt. Ltd.
- Experience: Varies by role (3–20 years)
- Qualification: B.Pharma / M.Pharma / M.Sc
- Location: Hinjewadi, Phase-II, International Biotech Park, Pune
- Work Type: On-site
Job Description
Centaur Pharmaceuticals is actively hiring seasoned professionals for multiple Quality Assurance roles in its regulatory Oral Solid Dosage (OSD) manufacturing facility in Pune. These positions are ideal for candidates with strong GMP exposure and a quality-first mindset who want to contribute to a dynamic, compliance-driven organization.
The openings focus on various aspects of QA, including audits, compliance, analytical QA, validation, documentation, and in-process QA, supporting high standards of regulatory excellence.
Audit and Compliance
- Department: Quality Assurance
- Market: Pharmaceutical (Regulatory Formulation – OSD)
- Role: Audit and Compliance
- Experience: 04-06 years and 12-20 years
- Education/Qualification: B.Pharma / M.Pharma
Analytical Quality Assurance (AQA)
- Department: Quality Assurance
- Market: Pharmaceutical (Regulatory Formulation – OSD)
- Role: Analytical Quality Assurance (AQA)
- Experience: 06-10 years
- Education/Qualification: B.Pharma / M.Pharma / M.Sc
Process & Cleaning Validation
- Department: Quality Assurance
- Market: Pharmaceutical (Regulatory Formulation – OSD)
- Role: Process & Cleaning Validation
- Experience: 08-10 years
- Education/Qualification: B.Pharma / M.Pharma
Document Control / Doc Cell
- Department: Quality Assurance
- Market: Pharmaceutical (Regulatory Formulation – OSD)
- Role: Document Control / Doc Cell
- Experience: 03-05 years
- Education/Qualification: B.Pharma / M.Pharma
IPQA
- Department: Quality Assurance
- Market: Pharmaceutical (Regulatory Formulation – OSD)
- Role: IPQA
- Experience: 06-10 years
- Education/Qualification: B.Pharma / M.Pharma / M.Sc
Skills/Qualifications
- Strong exposure to regulatory formulation (OSD) manufacturing in companies approved by USFDA, MHRA, and EU
- Mandatory experience handling regulatory audits such as USFDA, MHRA, and EU
- Solid understanding of GMP and quality systems
- Excellent attention to detail with a quality-first mindset
- Good documentation and communication skills
- Ability to thrive in a fast-paced, compliance-oriented environment
- Ambition to drive excellence and make a meaningful impact
Key Responsibilities
- Ensure compliance with regulatory standards and audit requirements
- Conduct and support internal & external audits (USFDA, MHRA, EU)
- Perform analytical quality assurance and process validation activities
- Manage documentation control and in-process quality assurance
- Support cleaning validation and related QA protocols
- Maintain high standards of quality and continuous improvement
Benefits/Perks
- Career growth in a reputed integrated pharmaceutical company
- Opportunities for learning and skill development in global regulatory environments
- Exposure to international audits and best practices
- Collaborative work culture focused on innovation and excellence
- Long-term professional stability with a growing organization
How to Apply
Interested candidates with relevant experience in QA jobs and regulatory pharmaceutical manufacturing should share their updated resume along with a recent passport-size photograph to hrpune@centaur.co.in.
You can also reach out via phone at 91-20-66739510 for more details.
Apply now and take the next step in your pharma jobs journey with Centaur Pharmaceuticals. Don’t miss this opportunity to grow with a company committed to quality and innovation.
For more pharmaceutical careers in India and similar openings, explore listings on Pharma Recruiter.
Why You Should Join
Joining Centaur Pharmaceuticals means becoming part of a credible, innovation-driven organization with a strong track record in regulatory compliance and global operations.
You will enjoy long-term career stability, continuous learning opportunities, and a supportive culture that values quality and excellence. Work in a modern facility while contributing to products that impact health across 120+ countries.
FAQs
Q1: What is the required experience for these QA jobs at Centaur Pharmaceuticals?
A: Experience varies by role, ranging from 3–5 years (Document Control) to 12–20 years (Senior Audit & Compliance). Most positions require 4–10 years.
Q2: Is prior USFDA, MHRA, or EU audit exposure mandatory?
? A: Yes, exposure to regulatory formulation (OSD) manufacturing and audits like USFDA, MHRA, and EU is mandatory for all listed positions.
Q3: What qualifications are needed for these pharmaceutical careers?
A: Candidates should hold B.Pharma, M.Pharma, or M.Sc qualifications, depending on the specific role.
Q4: How can I apply for the Centaur Pune QA openings?
A: Email your resume and recent passport-size photograph to hrpune@centaur.co.in or call 91-20-66739510.
