Associate Manager, Quality Assurance – CGT

Lonza; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A global life sciences company in Singapore seeks an Associate Manager, Quality Assurance to supervise quality operations in a cell and gene therapy facility. The ideal candidate has extensive experience in the pharmaceutical industry, holds a degree, and possesses strong knowledge of GMP compliance. This role involves supporting audits, ensuring quality processes, and mentoring team members. Competitive compensation and comprehensive benefits are offered.

Benefits

Competitive compensation

Comprehensive medical insurance

Company transport provided

Professional growth opportunities

Qualifications

• Extensive experience in the pharmaceutical/biotech industry.
• Hands-on experience with manufacturing activities.
• Good knowledge of GMP requirements.

Responsibilities

• Supervise Quality Assurance operations and compliance.
• Support regulatory inspections and customer audits.
• Plan and prioritize activities for quality operations.

Skills

Operations/ Validation / Quality Unit experience

Team player

Knowledge of quality management system

Meticulous and systematic

Education

Degree from a recognized institution

Job description

Associate Manager, Quality Assurance – CGT

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

As an Associate Manager, QA you will supervise the day-to-day Quality Assurance activities in accordance with approved SOPs / Policies.

Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation. Learn new skills and capabilities. Grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.

What you will get

• An agile career and dynamic working culture in a global life sciences leader.
• An inclusive and ethical workplace that values diversity and integrity.
• Competitive compensation programs that recognize high performance.
• Professional growth opportunities through cross-functional projects and global exposure.
• Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.
• Company transport provided from designated MRT locations to and from the Tuas site.
• Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits

What you will do

• Supervise the day-to-day operation of approved Quality Assurance SOPs and Policies for a cell and gene therapy contract manufacturing facility.
• Provide support in backroom/front room, participate and front in regulatory inspections and customer audits as required.
• Demonstrate mastery and knowledge of processes, recognized by colleagues as a source of expertise.
• Show strong understanding of advanced cGMP and develop others in understanding advanced cGMP.
• Be recognized by colleagues as a source of expertise in cGMP and compliance.
• Identify problems, troubleshoot and coordinate corrective action.
• Review more complex decisions with supervisor and other departments.
• Plan and prioritize activities for self and team without supervision.
• Communicate quality operations and compliance perspective effectively to management.
• Involve in global harmonization/efficiency projects; begin to lead aspects of global projects within specific areas.
• Understand and articulate company business strategy; maintain a broad view of the business, recognizing changes and trends in the relevant area.
• Own and lead special projects, often complex in nature.
• Make suggestions for cost savings.
• Other tasks as assigned by Manager/Director.

What we are looking for

• Extensive experience in Operations/ Validation / Quality Unit in the pharmaceutical / biotech industry.
• Degree from a recognized institution.
• Relevant QA Operations background from the biopharma environment.
• Hands‑on experience coordinating & interacting with internal departments on manufacturing activities.
• Good knowledge and experience of the practical and theoretical requirements of quality management system in a GMP facility.
• Meticulous and systematic.
• Team player, with strong focus on safety, quality and timelines.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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