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 looking for a QC Laboratory Associate to join the Quality Control department at GSK Jurong. This role supports the day-to-day management of laboratory equipment, ensures documentation meets GMP and data integrity standards, and contributes to continuous improvement initiatives within the lab. It's a great opportunity for early-career candidates — including fresh graduates — looking to build a strong foundation in pharmaceutical quality control within a global organization.
Why join us?
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.
