CQ Compliance Support (Contract)

Our Client is a leading global biopharmaceutical organisation committed to developing innovative medicines that improve patient outcomes and address critical healthcare needs.

This position is responsible for overseeing the defined Commissioning and Qualification (CQ) scope of allocated area or scope, ensuring targets related to schedule, safety and compliance are achieved by their reporting teams.

1. Provide additional support to the C&Q Manager and Compliance Lead to drive and align on topics related and/or supporting project C&Q Program.
2. Develop more detail implementation plans/strategies in accordance with the framework provided in C&Q Plan, Global Guidelines/SOPs.
3. Liaise with stakeholders to get an alignment on plans/strategies proposed. This will include (but not limited to) EPCM, Third party suppliers, End User and QA.
4. Ad-hoc supporter for other C&Q Leads for specific topics related to their scope.
5. Support digital platforms scope for the project.
6. As part of the C&Q team reporting to the Compliance Lead, the main responsibilities and tasks are (but not limited to):
7. Ensure that CQV activities are executed in accordance with the Commissioning and Qualification Execution Plan and supporting Plans.
8. Development of strategies and procedures that support their execution scope.
9. Support C&Q schedule activities.
10. Guiding C&Q documentation preparation effort to ensure correctness, completeness and alignment across different areas/systems in accordance with strategies agreed.
11. Lead meetings to fine-tune commissioning topics.
12. Support the control of changes.
13. Ensure that quality standards are followed during C&Q execution. No significant observations in external regulatory inspections for allocated process area.

1. Bachelor's degree in Engineering (Chemical, Mechanical, Process, or related discipline)
2. A relevant Third Level or Professional Qualification
3. Familiar with methodologies related with Risk Based Validation
4. Digital execution platforms experience (i.e. Kneat, Veeva, Valgenesis, etc.)
5. Experience with cGMP

Be part of the pioneer team in Singapore and play a unique role in building and shaping the organisation’s operations from the ground up. As one of the first team members, you’ll have greater visibility and influence, the opportunity to shape processes and ways of working, and the chance to take on broader responsibilities as the organisation grows. You’ll also gain valuable exposure to senior stakeholders, build strong cross-functional relationships and establish a career foundation within a growing global organisation. It’s an opportunity to be there from the beginning, make your mark and grow alongside the business.