QA Operations Coordinator

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, 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.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

The QA Operations Coordinator is responsible for supporting the Quality Assurance (QA) function by coordinating daily QA operations with

various functions, ensuring product quality compliance and on-time release of product. The QA Operations Coordinator is responsible for

managing, updating, controlling and archiving quality records and SOPs. Functions as a bridge between various functions to ensure timely

completion of training, and document accuracy.

This position reports to the QA Manager and is part of the QA team located in Singapore Tuas site and will be an on-site role.

What you will do:

• Managing cGMP documents, ensuring that the procedures, forms and records are reviewed and revised according to schedule, performing record archival and ensuring that cGMP records are organized and retained according to record retention periods.

• Ensuring that product labels are printed in accordance with approved product specifications and supporting batch record management by facilitating and coordinating the flow of batch records across different functions.

• Supporting training program by liaising closely with various functions to ensure timely completion of training, and other quality-related activities such as customer audits, ensuring that records and documents required are being consolidated as a form of audit preparation process.

Who you are:

• High School Diploma, GED or local equivalent
• Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos,graphic, etc. and technical writing skills (create and edit complex procedures)
• Possess effective time management and organizational skills; able to balance multiple priorities and having the ability to interact and communicate effectively with both internal and external stakeholders

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

• An industry in a manufacturing/lab environment with cGMP exposure