Regional CQV Director

1 month ago


Singapore Integrated Project Services Full time

At IPS, we are seeking a highly experienced Regional CQV Director to lead our growth efforts in APAC. This role reflects our dedication to delivering exceptional solutions while solidifying our position as a global industry leader. As a Regional CQV Director, you will be responsible for performing cGMP compliance-based services, including commissioning, qualification, validation, consulting, and more. You will also lead, mentor, train, and manage a team of compliance staff assigned to the respective regional office. Additionally, you will support business development activities, including sales calls, proposal writing, lead generation, and more.

Key qualifications and requirements include a Bachelor's degree in Engineering or a related discipline, 15+ years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA, and experience with cleaning, processes, computer systems, methods, and other validation activities and processes. You should also have detailed experience in the discipline of GMP/Validation with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validate processes and how they relate to regulatory requirements and cGMP regulations within the APAC/EU/US FDA and international Standards and guidance.

IPS is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. Through operational expertise and industry-leading knowledge, skill, and passion, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products. We are proud to be an affirmative action and equal opportunity employer.


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