Job Description

We are building a high-caliber CQV (Commissioning, Qualification and Validation) team for Pharma and Biotech facilities that will support global pharma projects, including multinational clients. You will work on complex validation programs, regulatory-facing projects, and large-scale facility qualifications at Global Level.


Experienced professionals (10–14 years) based in India who have hands-on expertise in commissioning, qualification and validation of:


Active Pharmaceutical Ingredients (API) equipment

Oral Solid Dosage (OSD) formulation equipment

Sterile / Injectable manufacturing equipment

Utility Systems (HVAC, PW, WFI, Clean Steam, Compressed Air, Nitrogen)

Manufacturing facility qualification & cleanroom validation


What We’re Looking For:

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