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 Quality Control Specialist is responsible for managing a team of QC associates and ensuring that QC routine operations are carried out as per plan.

This position reports to the Quality Control Manager and is part of the Quality department located in Singapore, 25 Tuas South Street 1  and will be an on-site role.

What you will do:

Leading/providing oversight in OOS investigation, deviation report writing and CAPA planningProvide general oversight on QC routine operations, ensuring that the product and raw material testing schedules are on-track with minimal backlogDriving adherence to quality KPI’s and ensure timely reporting of data and trend to relevant stakeholdersEnsure that validation of new QC laboratory equipment and method is performedDeveloping and maintaining specialized technical expertise in order to provide support for existing products and ongoing GxP operations as required

Who you are:

University graduate (Science) with reasonable work experience OR equivalent relevant work experiencePossess at least 3 to 5 years of experience working in a QC Laboratory environmentExtremely detail and accuracy-oriented with good written and verbal communication skillsExperience in writing Laboratory Investigation details, Deviation records with root cause analysis and Change Control recordsKnowledge and experience of a GxP environment or other regulated industry

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

Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, and technical writing skills (create and edit procedures)Reasonable laboratory experience operating laboratory equipment, i.e. UPLC, Endotoxin plate readers, pH meters, microbial testing etc.
#LI-SS3 #LI-Onsite

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.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.