C&Q Compliance Support (Pharmaceutical / Biotech)

KINGSFORCE MANAGEMENT SERVICES PTE LTD; Singapore; On-site; SGD 78,000 - 134,000; Full time

Job summary

KINGSFORCE MANAGEMENT SERVICES PTE LTD in Singapore is seeking a project-based C&Q professional to support the C&Q Manager and Compliance Lead in executing the programme.

You will develop implementation plans aligned with global guidelines, coordinate with EPCM and suppliers, guide documentation, and drive scheduling and change control while ensuring GMP and cGMP compliance.

Qualifications

• Bachelor's Degree in Chemical, Mechanical, Process Engineering or related discipline.
• Experience in C&Q / CQV / validation within pharma, biotech or GMP environments.
• Familiarity with risk-based validation methodologies.
• Experience with cGMP.
• Strong documentation, coordination and stakeholder management skills.

Responsibilities

• Support the C&Q Manager and Compliance Lead in executing the project C&Q programme.
• Develop implementation plans and strategies in line with C&Q plans, global guidelines and SOPs.
• Coordinate with EPCM, third-party suppliers, end users and QA.
• Ensure C&Q activities are executed in accordance with approved plans.
• Guide preparation and review of C&Q documentation.
• Support C&Q scheduling and change control activities.
• Lead meetings related to commissioning topics.
• Support digital C&Q platforms and compliance activities.
• Ensure quality and GMP standards are maintained throughout C&Q execution.

Skills

Documentation

Coordination

Stakeholder management

Education

Bachelor's Degree in Chemical, Mechanical, Process Engineering or related discipline

Tools

Kneat

Veeva

ValGenesis

Job description

About our client

Our client is a leading global pharmaceutical company.

About the role

• Support the C&Q Manager and Compliance Lead in executing the project C&Q programme
• Develop implementation plans and strategies in line with C&Q plans, global guidelines and SOPs
• Coordinate with EPCM, third-party suppliers, end users and QA
• Ensure C&Q activities are executed in accordance with approved plans
• Guide preparation and review of C&Q documentation
• Support C&Q scheduling and change control activities
• Lead meetings related to commissioning topics
• Support digital C&Q platforms and compliance activities
• Ensure quality and GMP standards are maintained throughout C&Q execution

About you

• Bachelor's Degree in Chemical, Mechanical, Process Engineering or related discipline
• Relevant experience in C&Q / CQV / validation within a pharmaceutical, biotech or GMP environment
• Familiarity with risk-based validation methodologies
• Experience with cGMP
• Experience with digital execution platforms such as Kneat, Veeva or ValGenesis is advantageous
• Strong documentation, coordination and stakeholder management skills
• Able to work within strict project deadlines
• Good written and spoken English

Other

• Employment Type: Project-based contract role
• Work Schedule: 5 days per week
• Location: Tuas, Singapore

*Please note that only shortlisted candidates will be contacted.*