
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.
The Lead HVAC & Cleanroom Engineer is responsible for the complete design, coordination, and implementation of HVAC and cleanroom systems across manufacturing and support buildings. This role ensures systems are designed and delivered in alignment with URS, cGMP, ISO cleanliness standards, and environmental requirements. It also provides technical guidance throughout procurement, installation, commissioning, and qualification. The engineer is accountable for ensuring CTOD and VTOD documentation are properly completed for system validation and handover.
Key Responsibilities
Review engineering deliverables and vendor submissions.
Provide technical support during procurement and installation.
Support commissioning, qualification, and validation readiness.
Ensure accurate CTOD/VTOD preparation for turnover.
Troubleshoot system performance issues during startup.
Required Qualifications
Degree in Mechanical Engineering or related field.
Experience with commissioning and qualification (C&Q) processes.
Excellent cross-functional coordination and documentation skills.
Why join us?
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.

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.