Centaur Pharmaceuticals is inviting applications from experienced pharmaceutical manufacturing professionals for multiple Quality Control and Quality Assurance positions at its Pune location. The hiring is focused on candidates with strong GMP exposure, a quality-first mindset, and the ambition to contribute to compliance, innovation and continuous growth.

These openings are suitable for candidates with experience in regulatory formulation OSD manufacturing companies and exposure to regulatory audits such as USFDA, MHRA and EU. Interested candidates can apply by email as per the instructions shared by the company.

1. Quality Control Roles

Job Overview

The Quality Control department is hiring for section head, officer and analyst-level roles across stability, AMV/AMT, RM, GLP and QC analysis functions. These positions require candidates with M.Sc qualification and relevant experience in pharmaceutical quality control operations.

Open Positions

Responsibilities

• Handle assigned Quality Control activities as per the role and section requirements.
• Support GMP-compliant laboratory and documentation practices in a pharmaceutical manufacturing environment.
• Contribute to audit readiness for regulatory inspections including USFDA, MHRA and EU audits.
• Maintain a quality-first approach while working within assigned QC sections such as stability, AMV/AMT, RM, GLP or QC analysis.

Qualifications

• M.sc qualification is required for the listed Quality Control positions.
• Candidates should have experience in regulatory formulation OSD manufacturing companies such as USFDA, MHRA and EU.

Key Skills and Experience Required

• 04-06 Yrs experience for QC Analyst role.
• 12-16 Yrs experience for Section Head roles.
• Exposure to regulatory audits like USFDA, MHRA and EU is required.
• Strong GMP exposure and a quality-first mindset are expected.

2. Quality Assurance Roles

Job Overview

The Quality Assurance department is hiring experienced candidates for Technology Transfer Development, QMS and Analytical Quality Assurance roles. These positions require B.Pharma / M.Pharma or M.Sc qualifications depending on the role and are intended for candidates experienced in regulated pharmaceutical manufacturing environments.

Open Positions

Responsibilities

• Support Quality Assurance activities for the assigned function, including Technology Transfer Development, QMS or Analytical Quality Assurance.
• Work in line with GMP expectations and compliance requirements for regulated pharmaceutical manufacturing.
• Contribute to regulatory audit preparedness and quality system effectiveness.
• Maintain documentation, coordination and quality practices relevant to the assigned QA role.

Qualifications

• B.Pharma / M.Pharma qualification is required for Technology Transfer Development.
• B.Pharma / M.Pharma / M.sc qualification is required for QMS and Analytical Quality Assurance (AQA).
• Candidates should have experience in regulatory formulation OSD manufacturing companies such as USFDA, MHRA and EU.

Key Skills and Experience Required

• 08-12 Yrs experience for Technology Transfer Development.
• 12-16 Yrs experience for QMS and Analytical Quality Assurance roles.
• Exposure to regulatory audits like USFDA, MHRA and EU.
• Strong GMP exposure and quality-first mindset.

Why This Role Is a Good Opportunity

Centaur Pharmaceuticals highlights this hiring as an opportunity for seasoned pharmaceutical manufacturing professionals to join an organization committed to innovation, compliance and continuous growth. The openings are relevant for candidates who want to work in core QA and QC functions in a regulated manufacturing environment.

How to Apply

Interested candidates can share their resume and recent passport size photograph on below given mail address.

hrpune@centaur.co.in

91-20-66739510

Location: Hinjewadi, Phase-II, International biotech park, Pune