Introduction

We are recruiting a Commissioning & Qualification - Manager to join one of our leading multinational clients and their expanding team. This position is Bangalore based in and offers an excellent opportunity for experienced proposal management professionals in the Life Science sector.

What are you going to do

Position: Commissioning & Qualification - Manager.

Contract: On Permanent Role.

Would be part of the Project team involved in making complex biopharma/Large API facilities
Driving the project with Science and Risk based Validation (SRV) concept.
Work very closely with our customers, Extensive Travelling Involved.
Have strong leadership qualities to lead a team of C&Q Engineers/Leads and aligning with Multiple stakeholders.
Have knowledge of process equipment’s systems
To drive C&Q activities with multiple stakeholders like (Engineering responsible, Design consultant, Vendor’s, and QA) of the project organization:
Align quality and validation concept with customer’s quality system & validation concept.
Define scope of C&Q activities in the project and scope of work within quality work package incl. relevant C&Q activities.
Ensure changes to scope are brought to the attention of Project Management.
Ensure interfaces to and coordination with other disciplines
Review work of project members in the quality work package.
Generate validation deliverables like IQ, OQ, PQ protocols and reports, etc.
Act as Smarter Execution consultant for Project Members.
Ensure C&Q documentation is in compliance with GMP and GEP (incl. ASTM E2500).
Conduct follow-up on QAP, Project execution Plan on C&Q activities
Having work experience on QMS based Project environment

Essential skills and knowledge

Bachelor’s or master’s degree in a relevant science, engineering, or pharmaceutical field.
15+ years’ experience performing commissioning and / or qualification activities in an FDA regulated industry.
Ideally you will already have experience in equipment qualification.
Should have knowledge with recent edition of ISPE C&Q and GAMP and regulatory guidelines USFDA, EU GMP, Annexure 11 & 21 CFR 11 and ICH guidelines.

What we offer

Why work with Brunel? We take pride in offering exciting career opportunities through our network of 120+ offices across 40+ countries. We understand that advancing your career requires dedication and the right support—let us match you with your ideal position in the energy sector.

Closing: November 09, 2025

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Do you have any questions about this vacancy?

Vacancy reference: PUB415119

SP

Corporate recruiter

Saumya Poojari

Contact

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