CQ Manager - QC Laboratory

No deviation; Singapore; On-site; SGD 80,000 - 120,000; Full time

Job summary

A leading pharmaceutical consultancy in Singapore is seeking a CQ Manager QC Laboratory to lead the commissioning and qualification of analytical laboratories. You will collaborate with cross-functional teams to ensure compliance with GMP standards while overseeing the installation and validation of laboratory systems. The ideal candidate has over 10 years of CQV experience and a degree in Life Sciences, Chemistry, or Engineering, along with strong knowledge of analytical instrumentation and lab compliance.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• 10+ years CQV experience in QC labs.
• Strong knowledge of analytical instrumentation and lab software validation.
• Experience with GMP and regulatory standards.

Responsibilities

• Lead commissioning and qualification of analytical laboratories.
• Ensure compliance with GMP, ALCOA+, and data integrity standards.
• Maintain audit-ready documentation and inspection readiness.

Skills

CQV experience

Analytical instrumentation knowledge

GMP compliance

Lab software validation

Education

Degree in Life Sciences, Chemistry, or Engineering

Job description

About No deviation

At No deviation, we are dedicated to delivering patient‑centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

We are seeking a knowledgeable CQ Manager QC Laboratory to lead commissioning and qualification of analytical laboratories that support critical testing and quality assurance operations. You will oversee installation, commissioning, and validation of analytical instruments, stability chambers, and laboratory systems, ensuring compliance with GMP, ALCOA+, and data integrity standards. You will collaborate closely with QC, QA, and Engineering teams, manage vendors, and maintain audit‑ready documentation. This role is key in guaranteeing the accuracy, reliability, and compliance of laboratory testing for pharmaceutical products.

Key Responsibilities

• CQV for HPLC/UPLC, GC, LC‑MS, PCR, stability chambers, and environmental monitoring systems.
• Oversee commissioning of lab equipment, instruments, and software (LIMS/CSV).
• Ensure compliance with GMP, ALCOA+, and data integrity standards.
• Collaborate with QC, QA, Engineering, and vendors.
• Maintain audit‑ready documentation and inspection readiness.

Required Qualifications

• Degree in Life Sciences, Chemistry, or Engineering.
• 10+ years CQV experience in QC labs.
• Strong knowledge of analytical instrumentation, GMP, and lab software validation.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.