Centaur Pharmaceuticals is inviting applications from experienced pharmaceutical professionals for multiple positions in the Quality Control (QC) and Quality Assurance (QA) departments at its Hinjewadi facility in Pune, Maharashtra. The company is looking for skilled candidates with strong pharmaceutical manufacturing experience, knowledge of Good Manufacturing Practices (GMP), and exposure to regulatory audits.

This recruitment drive offers opportunities for experienced professionals seeking career growth in pharmaceutical quality control, quality assurance, analytical testing, and technology transfer.

Job Details

Company Name: Centaur Pharmaceuticals
Job Location: Hinjewadi, Phase II, International Biotech Park, Pune, Maharashtra
Departments: Quality Control (QC) and Quality Assurance (QA)
Industry: Pharmaceutical Manufacturing
Experience Required: 4–16 years, depending on the position
Application Mode: Email

1. Quality Control (QC) Vacancies

The following positions are available in the Quality Control department:

• Assistant Manager / Deputy Manager – Stability Section Head: M.Sc. qualification with 12–16 years of experience.
• Assistant Manager / Deputy Manager – AMV / AMT Section Head: M.Sc. qualification with 12–16 years of experience.
• Assistant Manager / Deputy Manager – RM Section Head: M.Sc. qualification with 12–16 years of experience.
• Assistant Manager / Deputy Manager – GLP Section Head: M.Sc. qualification with 12–16 years of experience.
• Officer / Senior Officer – QC Analyst: M.Sc. qualification with 4–6 years of experience.

2. Quality Assurance (QA) Vacancies

The following opportunities are available in the Quality Assurance department:

• Executive / Senior Executive – Technology Transfer Development: B.Pharma or M.Pharma qualification with 8–12 years of experience.
• Assistant Manager / Deputy Manager – Quality Management System (QMS): B.Pharma, M.Pharma, or M.Sc. qualification with 12–16 years of experience.
• Assistant Manager / Deputy Manager – Analytical Quality Assurance (AQA): B.Pharma, M.Pharma, or M.Sc. qualification with 12–16 years of experience.

Eligibility Criteria

Candidates should have relevant experience in pharmaceutical manufacturing, particularly in regulatory formulation (OSD) manufacturing companies. Experience working with regulated markets such as the USFDA, MHRA, and EU is preferred or required as indicated in the recruitment notice.

Applicants should have a good understanding of GMP requirements, pharmaceutical quality systems, documentation practices, and regulatory compliance. Experience in regulatory audits conducted by agencies such as USFDA and MHRA is mandatory according to the advertisement.

Candidates should apply for positions matching their qualifications, experience, and technical expertise.

Key Responsibilities

Depending on the selected position, responsibilities may include:

• Managing pharmaceutical quality control and quality assurance activities.
• Supervising stability studies and maintaining stability-related documentation.
• Performing or overseeing analytical testing of raw materials and pharmaceutical products.
• Supporting analytical method validation and analytical method transfer.
• Ensuring compliance with GMP and applicable regulatory requirements.
• Managing quality management systems, deviations, CAPA, change control, and audit documentation.
• Supporting technology transfer and process development activities.
• Preparing for regulatory inspections and maintaining audit readiness.

How to Apply

Interested and eligible candidates should send their updated resume along with a recent passport-size photograph to the recruitment email address provided below.

Email: hrpune@centaur.co.in
Contact Number: 91-20-66739510
Location: Hinjewadi, Phase II, International Biotech Park, Pune, Maharashtra

Applicants should mention the position and department in the email subject line. Ensure that your resume clearly highlights your relevant pharmaceutical experience, technical skills, regulatory exposure, and qualifications.

Note: The recruitment advertisement does not specify a last date for applications. Candidates should contact the company to confirm current vacancies and further recruitment details.

5 Technical FAQs

1. What technical experience is required for Centaur Pharmaceuticals QC jobs?

Candidates applying for QC positions should have relevant pharmaceutical analytical experience. Depending on the role, knowledge of stability studies, raw material testing, analytical method validation, analytical method transfer, laboratory documentation, and GMP compliance may be required.

2. What is the importance of stability studies in pharmaceutical manufacturing?

Stability studies evaluate how the quality of a pharmaceutical product changes over time under specified environmental conditions. They help establish shelf life, storage conditions, and expiry dates in accordance with applicable regulatory requirements.

3. What are analytical method validation (AMV) and analytical method transfer (AMT)?

Analytical method validation demonstrates that an analytical procedure is suitable for its intended purpose. Analytical method transfer evaluates whether a validated method can be transferred successfully between laboratories while maintaining reliable and consistent results.

4. What technical knowledge is required for Quality Assurance and QMS positions?

Candidates should understand GMP, deviation management, corrective and preventive actions (CAPA), change control, document control, internal audits, and quality risk management. Knowledge of applicable regulatory requirements and pharmaceutical quality systems is important.

5. Why is regulatory audit experience important for these positions?

Regulatory audit experience helps professionals understand inspection procedures, maintain compliant documentation, identify quality gaps, and support corrective actions. Familiarity with USFDA, MHRA, and EU regulatory expectations is valuable for pharmaceutical facilities supplying regulated markets.

Conclusion

Centaur Pharmaceuticals offers opportunities for experienced professionals in Quality Control and Quality Assurance at its Pune facility. Candidates with suitable qualifications, strong technical knowledge, GMP experience, and regulatory audit exposure can apply by submitting their updated resume to the recruitment email address.

Interested candidates should verify vacancy availability and role-specific requirements directly with the company before applying.