CQV Manager – Projects / Singapore / China

CQV Manager / Lead – Projects

Location: Singapore / China

Industry: Life Sciences / Pharmaceutical Manufacturing

Role Overview

We are seeking a highly skilled CQV (Commissioning, Qualification & Validation) Manager to lead and deliver large-scale greenfield projects in the Life Sciences sector. This permanent position requires strong leadership, technical expertise, and bilingual proficiency to manage complex validation programs and ensure compliance with global standards.

Key Responsibilities

• Lead the commissioning and validation of large greenfield projects.
• Manage and mentor large cross-functional teams, including Process, Facilities/Utilities, and Automation C&Q groups.
• Oversee commissioning and validation activities using process automation systems for process equipment.
• Develop and review validation protocols (IQ, OQ, PQ) for process equipment.
• Interface effectively with client personnel and external vendors to ensure smooth project execution.
• Manage all facets of assigned validation projects, maintaining clear communication with client representatives on project status, risks, and support needs.
• Drive compliance with GMP, FDA, EMA, and global regulatory standards .
• Ensure robust documentation and execution of Electronic Validation systems .

Key Attributes

• Strong leadership and project management skills.
• Excellent communication and stakeholder management abilities.
• Ability to work in a fast-paced, regulated environment.
• Proficiency in English and Chinese (mandatory).
• Expertise in Electronic Validation tools and systems .

Qualifications

• Bachelor’s or Master’s degree in Engineering, Life Sciences, or related discipline .
• Extensive experience in CQV project management within the Life Sciences industry.
• Proven track record in greenfield project execution and managing large validation teams.
• Strong knowledge of automation systems, utilities, and process equipment validation .
• Hands-on experience with protocol development and review (IQ/OQ/PQ) .

This JD positions the role as a senior leadership opportunity for professionals with bilingual proficiency and deep CQV expertise, emphasizing greenfield project delivery and electronic validation systems.

Would you like me to also create a short recruiter-style outreach pitch (under 300 characters) for LinkedIn InMail, so you can quickly attract candidates alongside this full JD?

rewrite this jD company name as AMTSOL

Here’s the rewritten Job Description with AMTSOL as the company name:

CQV Manager – Projects (Permanent Role)

Company: AMTSOL Industry: Life Sciences / Pharmaceutical Manufacturing

Role Overview

AMTSOL is seeking a highly skilled CQV (Commissioning, Qualification & Validation) Manager to lead and deliver large-scale greenfield projects in the Life Sciences sector. This permanent position requires strong leadership, technical expertise, and bilingual proficiency to manage complex validation programs and ensure compliance with global standards.

Key Responsibilities

• Lead the commissioning and validation of large greenfield projects.
• Manage and mentor large cross-functional teams, including Process, Facilities/Utilities, and Automation C&Q groups.
• Oversee commissioning and validation activities using process automation systems for process equipment.
• Develop and review validation protocols (IQ, OQ, PQ) for process equipment.
• Interface effectively with client personnel and external vendors to ensure smooth project execution.
• Manage all facets of assigned validation projects, maintaining clear communication with client representatives on project status, risks, and support needs.
• Drive compliance with GMP, FDA, EMA, and global regulatory standards .
• Ensure robust documentation and execution of Electronic Validation systems .

Key Attributes

• Strong leadership and project management skills.
• Excellent communication and stakeholder management abilities.
• Ability to work in a fast-paced, regulated environment.
• Proficiency in English and Chinese (mandatory).
• Expertise in Electronic Validation tools and systems .

Qualifications

• Bachelor’s or Master’s degree in Engineering, Life Sciences, or related discipline .
• Extensive experience in CQV project management within the Life Sciences industry.
• Proven track record in greenfield project execution and managing large validation teams.
• Strong knowledge of automation systems, utilities, and process equipment validation .
• Hands-on experience with protocol development and review (IQ/OQ/PQ) .