Manager, Quality Control

SCIEX; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading life sciences firm in Singapore is seeking a Quality Control Manager to oversee daily operations, ensuring timely inspection of materials. The role involves implementing ISO compliant processes and collaborating with cross-functional teams to improve quality standards. Candidates should have a Bachelor's degree in engineering with 3-5 years of quality-related experience, including people management. This position offers a competitive salary and potential bonuses, contributing to impactful innovations in the field.

Benefits

Health care program

Paid time off

Bonus/incentive pay

Qualifications

• 3-5 years in quality-related functions, preferably in manufacturing or medical devices.
• 1-2 years of people management experience.
• Knowledge of ISO standards and FDA QSR.

Responsibilities

• Oversee daily operations of the Quality Control team.
• Implement quality processes aligned with ISO 9001 and FDA regulations.
• Collaborate with cross-functional teams to resolve quality issues.

Skills

Quality control

Problem-solving tools

Education

Bachelor's degree in engineering

Job description

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At SCIEX, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
As part of SCIEX, you will help to influence life changing research and outcomes, while accelerating your potential. For more than 50 years, we have been empowering our customers to solve the most impactful analytical challenges in quantitation and characterization through ground-breaking innovation and outstanding reliability and support. You will be part of a winning team, enabled by DBS, that is passionate about helping life science experts around the world get to answers they can trust.
Learn about the Danaher Business System which makes everything possible.

In This Role, You Will Have The Opportunity To

• Oversee daily operations of the Quality Control team, ensuring timely and accurate inspection of incoming materials and components.
• Implement and maintain quality processes aligned with ISO 9001, ISO 13485, and US 21 CFR 820 requirements, participate and support internal and external audits.
• Collaborate with cross-functional teams (Sourcing/Buyer, Planning, Manufacturing, R&D, QA) to resolve quality issues (e.g., NCMR, Complaints, etc) and drive continuous improvement to close process gaps by applying problem‑solving tools (e.g., 5WHY, Fishbone, 8D, etc).
• Provide training and guidance to team members and third‑party logistics inspectors on quality standards and processes.
• Support Senior Leadership team by sponsoring innovative ideas to improve Quality operation, by recommending, supporting, and implementing continuous improvement activities in processes, to optimize results to improve quality of delivery, meeting quality standards requirements deliverable according with Company and Customer requirements.
• Collaborating and gathering data to identify and interpret performance trends/metrics, analyze, summarize, and communicate pertinent information to management. Ensure timely, accurate and complete data reporting, ensuring alignment with business objectives.
• Implement benchmark and best‑practice activities in all areas of responsibilities to maintain exceptionally high levels of quality and compliance across the Danaher OpCos.

The Essential Requirements Of The Job Include

• Bachelor's degree in engineering
• 3–5 years in quality‑related functions, preferably in manufacturing or medical devices with knowledge of ISO standards, FDA QSR, and quality system principles.
• 1–2 years of people management experience.
• Experience with audits and regulatory compliance.
• Ability to work in a highly matrixed and geographically diverse business environment preferred.

Travel, Motor Vehicle Record & Physical/Environment Requirements

• Ability to travel –5% travel, overnight, within territory or occasional international travel

It would be a plus if you also possess previous experience in:

• Medical Device Industry
• Professional designations not required but training and certification in quality or regulatory affairs are a plus (e.g. CQM, CQE, CQA, RAC, Six sigma, Lean)

SCIEX, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. This job is also eligible for bonus/incentive pay.
Join our winning team today. Together, we’ll accelerate the real‑life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.