Senior CQV Manager - Pharmaceutical Manufacturing

Turner & Townsend

Singapore

On-site

SGD 190,000 - 270,000

Full time

22 hours ago
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Job summary

Turner & Townsend is a global professional services company delivering outcomes across real estate, infrastructure, energy and natural resources. We are seeking an experienced CQV Manager for a major pharmaceutical manufacturing project in Singapore, to lead commissioning, qualification and startup activities through a full project lifecycle.

The ideal candidate has 15+ years of CQV experience with strong leadership, regulatory knowledge (FDA/EMA/GMP) and a proven track record on large

Qualifications

  • Bachelor's Degree in Engineering, Pharmaceutical Sciences, Life Sciences or related field.
  • Minimum 15 years of CQV experience on large-scale pharmaceutical projects.
  • Experience leading CQV on greenfield pharmaceutical manufacturing projects.
  • Experience in GMP-regulated facilities and regulatory standards.
  • Experience in Singapore-based pharmaceutical capital projects is highly desirable.

Responsibilities

  • Develop and implement commissioning strategies and master plans.
  • Lead CQV planning and execution across process, utility, facility and automation.
  • Prepare qualification/verification protocols and documentation.
  • Oversee FATs, SATs, turnover and system handover activities.
  • Collaborate with Engineering, Process, Automation, Construction, Quality and Operations.
  • Support startup and operational readiness activities.

Skills

CQV leadership
GMP knowledge
Project management
Stakeholder management
Team leadership
Communication

Education

Bachelor's Degree in Engineering, Pharmaceutical Sciences, Life Sciences

Tools

Process equipment & utilities
Automation systems
Validation protocols

Job description

Turner & Townsend is a global professional services company delivering outcomes across real estate, infrastructure, energy and natural resources. We are seeking an experienced CQV Manager for a major pharmaceutical manufacturing project in Singapore, to lead commissioning, qualification and startup activities through a full project lifecycle.

The ideal candidate has 15+ years of CQV experience with strong leadership, regulatory knowledge (FDA/EMA/GMP) and a proven track record on large

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