Centaur Pharmaceuticals is inviting applications for Officer / Sr. Officer – QA (ITQA) positions for its pharmaceutical manufacturing operations. The role focuses on Computer System Validation (CSV), GMP systems, validation documentation, CAPA, change control and regulatory audit support.

Candidates with relevant experience in pharmaceutical manufacturing, particularly regulatory formulation (OSD) manufacturing, and exposure to audits such as USFDA, MHRA and EU are encouraged to apply through the email address provided in the recruitment notification.

Centaur Pharma QA ITQA Recruitment 2026 – Overview

About the Role

The selected candidates will work within the QA-ITQA function and will be responsible for ensuring that computerized systems and GMP-related processes meet applicable validation and compliance requirements.

The position involves documentation, validation lifecycle activities, risk assessments, CAPA tracking, change controls and support for internal, external, vendor and regulatory audits.

Roles & Responsibilities

Key responsibilities mentioned in the recruitment notification include:

• Responsible for Computer System Validation (CSV) for GMP instruments.
• Develop, manage and review GxP system lifecycle documentation.
• Prepare and review Validation Plans and User Requirements Specifications (URS).
• Handle Functional and Design Specifications and testing protocols including IQ/OQ/PQ.
• Prepare and maintain Traceability Matrices, Validation Reports and SOPs.
• Manage Change Control documentation.
• Perform and support risk assessments and validation summary reports.
• Monitor and track applicable Corrective and Preventive Actions (CAPA).
• Follow up and resolve comments, deviations and technical issues.
• Support internal, external, vendor and regulatory audits.

Eligibility & Required Experience

Centaur’s notification specifically highlights candidates with experience in regulatory formulation (OSD) manufacturing companies.

Candidates should have:

• Relevant experience in the pharmaceutical manufacturing environment.
• Experience/exposure to USFDA, MHRA and EU regulatory audits.
• Understanding of GMP systems and computerized system validation.
• Relevant experience in QA/ITQA validation activities.

Important: The recruitment notification does not specify a particular educational qualification, so no degree has been assumed in this article.

Regulatory & Compliance Exposure

Exposure to regulatory audits is specifically highlighted as mandatory in the notification, including:

• USFDA
• MHRA
• European Union (EU)

This makes the opportunity particularly relevant for professionals with pharmaceutical manufacturing and regulatory compliance exposure.

Salary & Benefits

Salary: Not disclosed by Centaur Pharmaceuticals in the provided recruitment notification.

The exact compensation for the Officer/Sr. Officer position will depend on the candidate’s experience, skills and organizational pay structure. A realistic market-oriented range for comparable QA/ITQA roles may be around ₹4.5 lakh to ₹8 lakh per annum, but candidates should confirm the actual CTC during the recruitment process.

Other benefits, if applicable, will be communicated by the company during the selection process.

Selection Process

The notification does not specify a detailed selection process. Candidates may be evaluated based on their:

• Relevant pharmaceutical manufacturing experience
• QA/ITQA and CSV knowledge
• GMP and validation experience
• Regulatory audit exposure
• Technical and documentation skills

How to Apply

Interested and eligible candidates can apply by sending their updated resume and recent passport-size photograph to the email address mentioned in the recruitment notification.

Email: hrpune@centaur.co.in

Candidates should ensure that their resume clearly highlights relevant experience in CSV, GMP systems, validation, QA/ITQA and regulatory audits.