No deviation

CQ Manager - Utilities

No deviation  •  Singapore, SG (Onsite)  •  2 days ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

We are seeking an experienced CQ Manager Utilities
to lead the commissioning and qualification of critical utility systems supporting multiple manufacturing facilities. You will oversee WFI/PW systems, clean steam, HVAC, boilers, chillers, and compressed gas distribution to ensure they meet operational, regulatory, and GMP requirements. In this role, you will coordinate with Engineering, QA, and external vendors, troubleshoot issues during startup, and maintain audit-ready documentation. Your contributions will ensure reliable and compliant utility support to produce high-quality pharmaceuticals.

Key Responsibilities

  • Lead CQV activities for WFI/PW systems, clean steam, HVAC, chillers, boilers, compressed air, nitrogen, and utility distribution systems.
  • Develop and execute commissioning plans, IQ/OQ protocols, and utility validation documentation.
  • Ensure utilities meet capacity, quality, and regulatory requirements.
  • Troubleshoot engineering and performance issues during startup.
  • Partner with Engineering, Facilities, QA, Automation, and external contractors.
  • Drive system impact assessments, risk assessments, deviations, and change controls.
  • Ensure utility systems are continuously audit-ready.

Required Qualifications

  • Degree in Mechanical, Chemical, Electrical Engineering, or equivalent.
  • 10+ years CQV experience with GMP utilities in pharma/biotech.
  • Strong technical knowledge of water systems, HVAC, and clean utility design.
  • Familiarity with regulatory requirements for critical utilities (FDA/EU/PICS).

Why join us?

  • Generous Leave Policy.
  • Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
  • Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
  • Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
  • Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

No deviation

About No deviation

Founded in 2007, No deviation is a trusted partner to pharmaceutical and biotech companies seeking smarter ways to deliver compliance. From engineering consultancy to CQV execution, regulatory compliance, and digital enablement, we support our clients across the entire project lifecycle in Asia, Europe.

We specialise in:

CQV (Commissioning, Qualification & Validation)

Lean, risk-based approaches aligned with GAMP 5, Annex 15, and ASTM E2500.

Quality, Compliance & Regulatory

Audit readiness, QMS remediation, documentation, and training.

Project Management & Technical Support

From operational readiness to vendor coordination.

Digital Enablement

Implementation of paperless validation (e.g. Kneat Gx), data integrity, and process digitalisation.

Specialised Training & Talent Support

Upskilling programs and resource placement to accelerate project success.

Our approach is rooted in patient safety, process understanding, regulatory compliance, and a constant drive for operational excellence in terms of safety, quality, delivery, and cost.

If you’re troubleshooting a deviation, planning a major CQV deployment, or scaling digital validation tools, we work side-by-side with your teams to deliver meaningful outcomes. Our methodology draws from ICHQ9 risk principles, with a hands-on framework: Understand - Observe - Define - Implement.

Want to learn more about paperless CQV, digital QMS, or project-ready resources? We’re happy to talk. Visit nodeviation.com to explore how we can support you.

Industry
Chemicals & Materials
Company Size
51-200 employees
Headquarters
Singapore, SG
Year Founded
2007
Social Media