CQV Manager: Drug Linker & GMP Systems

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 80,000 - 110,000; Full time

Job summary

A pharmaceutical solutions provider in Singapore is seeking a CQ Manager Drug Linker to oversee the commissioning and qualification of chemical synthesis equipment. Candidates should have over 10 years of CQV experience in relevant environments and a degree in chemical engineering or chemistry. This role ensures compliance with GMP standards and requires coordination with multiple teams. The company offers benefits like generous leave, health coverage, and professional development opportunities.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• 10+ years of CQV experience in chemical synthesis preferred.
• Knowledge of GMP requirements and solvent-based systems required.
• Strong technical understanding of bioconjugation equipment is a plus.

Responsibilities

• Lead CQV activities for chemical synthesis and conjugation equipment.
• Develop and execute CQ deliverables: URS, risk assessments, IQ/OQ/PQ.
• Ensure compliance with GMP and safety guidelines for highly potent materials.

Skills

CQV experience in chemical synthesis

Knowledge of containment requirements

Strong technical understanding of linker synthesis

Education

Degree in Chemical Engineering, Chemistry, or related discipline

Job description

A pharmaceutical solutions provider in Singapore is seeking a CQ Manager Drug Linker to oversee the commissioning and qualification of chemical synthesis equipment. Candidates should have over 10 years of CQV experience in relevant environments and a degree in chemical engineering or chemistry. This role ensures compliance with GMP standards and requires coordination with multiple teams. The company offers benefits like generous leave, health coverage, and professional development opportunities.