Sanjay has over 20 years of rich and diversified experience in Project Delivery, Process Design, Commissioning, Qualification & Validation (CQV) of Pharmaceutical, Biological, Vaccine, Plasma & Cohn Fractionation, OSD, bulk API Projects, & FMCG. 

He is Proficient in driving project from start to completion, through its entire Life Cycle – starting from inception, feasibility, concept, detailed design; followed by commissioning, validation, and final handover. Delivered multiple Big & Small Cap projects successfully across Pharma-Bio Sector in Singapore, Malaysia, USA, Ireland, and India region.

He is experienced in delivering large capital international projects, involving multi-office and multi-cultural environment for big Pharmaceutical MNC companies successfully. He is excellent team player, understands project goal, built strong relationship with project sponsors, and works closely to manage all stakeholder expectations. Tenacity, flexibility, and resourcefulness are a few of the characteristics that he has developed while successfully delivering various greenfield and brownfield projects to clients

In past two years, he has delivered various small and medium capital projects for clients, such as MSD, Amgen, Pfizer, GSK, and Lonza in Singapore Market. He is responsible to understand sponsor and stakeholder requirements and communicating same clearly to design and engineering team, manage contractual and legal obligations, ensuring compliance to quality, safety, and environment policies. Identify and mitigate all risks in the Project. Plan activity and resource; develop and control schedule. Monitoring project progress, controlling project change, preparing, and managing project budget, mitigating adverse trends related to cost and schedule.

Through his previous experience working as CQV lead with industry-leading multinational corporations on various projects, he has gained strong knowledge and well versed with latest cGMP regulatory requirements (FDA, WHO-GMP, UKMHRA, HSA, USFDA standards/ guidelines), ASME BPE standards, Good Documentation requirement and Good Engineering practices that are essential for Pharma industry. 

Over a time, he has gained good understanding of Local authority permitting requirements for Singapore, Sustainability, Green Mark, Buildability, Constructability, Design for Safety (DfS) etc.