Global Pharmaceutical Compliance Expert

4 weeks ago


Singapore Integrated Project Services Full time

Role Overview

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The Regional CQV Director will lead our growth efforts in Singapore, a newly created role reflecting IPS dedication to delivering exceptional solutions while solidifying its position as a global industry leader.

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This senior leadership position reports directly to the Managing Director, Matthew Shippey, with extensive experience in the pharmaceutical, data center, renewable energy, and manufacturing sectors. He brings a visionary approach and business-oriented mindset, driving exceptional results, and we seek an experienced professional to join this new exciting growth journey.

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Main Responsibilities

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  • Lead cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) developed and defined in project agreements with IPS clients.">
  • Mentor, train, and manage a team of compliance staff assigned to the respective regional office.">
  • Support business development activities including sales calls, proposal writing, lead generation, etc.">
  • Track staff utilization, coordinate staff assignments to projects, and assist in identifying, recruiting, interviewing, and hiring compliance staff.">
  • Maintain client relationships and be responsible for the overall delivery of projects in the assigned region, following IPS and client standards and requirements, good industry practices for C/Q/V services, and regulatory requirements.">
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Requirements

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We are seeking an experienced professional with:

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  • Bachelor's degree in Engineering or a related discipline or an equivalent technical degree.">
  • 15+ years of experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA, with expertise in writing and executing PFC, FC, IQ, OQ, and PQ forms and protocols for GMP Utilities, Equipment, Systems, and Software.">
  • Detailed experience in GMP/Validation, with 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 (ASTM, ICH, ISPE, etc.).">
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About Us

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IPS is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries. With over 3,000 professionals across 17 countries, IPS provides consultancy services, architecture, engineering, project controls, construction management, and compliance services that allow clients to develop and manufacture life-impacting products.

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Our newest acquisition, Linesight, specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industries.

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We offer a competitive salary range of $160,000 - $220,000 per annum, depending on qualifications and experience, plus benefits such as health insurance, retirement plan, and professional development opportunities.



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