CQ Manager – Drug Product, Aseptic Fill-Finish Lead

No deviation; Singapore; On-site; SGD 100,000 - 130,000; Full time

Job summary

A leading pharmaceutical consultancy in Singapore is seeking an experienced CQ Manager for their sterile fill-finish facility. The role involves leading cross-functional teams to ensure compliance with GMP standards while managing commissioning and qualification processes. Candidates should possess a degree in Engineering or Pharmaceutical Sciences and have over 10 years of experience in CQV within aseptic environments. This position offers professional development and a generous health benefits package.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• 10+ years of CQV experience in sterile fill-finish or aseptic manufacturing.
• Familiarity with isolator technology and Annex 1 requirements is required.
• Strong understanding of GMP and aseptic processing standards.

Responsibilities

• Lead CQV activities for isolators and cleanrooms.
• Execute protocols (FAT/SAT) and ensure compliance with regulatory standards.
• Collaborate with various departments to resolve equipment issues.

Skills

CQV experience

Aseptic processing

Problem-solving

Risk assessment

Education

Degree in Engineering or Pharmaceutical Sciences

Tools

Lyophilizers

Packaging equipment

Isolators

Job description

A leading pharmaceutical consultancy in Singapore is seeking an experienced CQ Manager for their sterile fill-finish facility. The role involves leading cross-functional teams to ensure compliance with GMP standards while managing commissioning and qualification processes. Candidates should possess a degree in Engineering or Pharmaceutical Sciences and have over 10 years of experience in CQV within aseptic environments. This position offers professional development and a generous health benefits package.