C&Q Compliance Support

QCS Staffing Ltd; Singapore; On-site; SGD 90,000 - 140,000; Full time

Job summary

QCS Staffing Ltd in Singapore is seeking a C&Q Compliance Support to assist a major biopharmaceutical project. You will help ensure CQV activities align with plans, develop strategies, and support schedule delivery within GMP standards.

The role requires a Bachelor's in Engineering, RBV experience, and familiarity with digital validation tools like Kneat, Veeva or ValGenesis, with the ability to work under tight deadlines.

Qualifications

• Bachelor's degree in Engineering or related discipline.
• RBV methodologies experience.
• Experience in GMP-regulated life sciences environments.

Responsibilities

• Ensure CQV activities are executed per the Execution Plan and project plans.
• Develop and implement C&Q strategies, procedures, and execution methodologies.
• Support planning, coordination, and delivery of C&Q schedule activities to meet milestones.
• Lead preparation of C&Q documentation with accuracy and alignment across systems.
• Facilitate cross-functional meetings to drive alignment on commissioning, qualification, and compliance.

Skills

RBV methodologies

GMP environments

Deadline management

Education

Bachelor's degree in Engineering or related

Tools

Kneat

Veeva

ValGenesis

Job description

C&Q Compliance Support – Singapore – Initial 24-Month Contract – Life Sciences

How would you like the opportunity support one of the largest biopharmaceutical projects in the country? If yes, then this is the assignment for you!

Our client is currently seeking the skills of a C&Q Compliance Support to assist their team. Our client develops and delivers life changing medicines to millions of people globally and as part of their growth. With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!

What You’ll Deliver

• Ensure CQV activities are executed in accordance with the Commissioning & Qualification Execution Plan and associated project plans.
• Develop and implement C&Q strategies, procedures, and execution methodologies within the assigned scope.
• Support the planning, coordination, and delivery of C&Q schedule activities to meet project milestones.
• Lead and guide the preparation of C&Q documentation, ensuring accuracy, completeness, consistency, and alignment across systems and functional areas.
• Facilitate cross-functional meetings to drive alignment on commissioning, qualification, and compliance activities, while supporting change control processes and maintaining GMP compliance standards.

Experience required:

• Bachelor's degree in Engineering or a related discipline.
• Relevant professional or higher-level qualification.
• Experience with Risk-Based Validation (RBV) methodologies.
• Ability to work effectively under tight project deadlines.
• Experience with digital validation platforms (e.g., Kneat, Veeva, ValGenesis).
• Knowledge of GMP-regulated pharmaceutical, biotech, or life sciences environments.