Be part of something altogether life-changing!
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. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Quality Control Analyst for Cytiva is responsible for sampling and inspection on raw materials, in-process materials, and finished products to ensure that product specifications and company and regulatory requirements are met, and release on a timely basis to meet on time delivery to our customers.
This position is part of the Quality Control team located in Global Life Sciences Solutions Singapore Pte Ltd, 25 Tuas South Street 1, Singapore 638034 and will be working on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.
In this role, you will have the opportunity to:
- Upkeeping and maintaining 5S and housekeeping in QC laboratory
- Performing raw materials inspection and sampling
- Inspecting or performing testing on raw materials, finished products conforming to production specifications in compliance with documented procedures and in accordance to stipulated deadlines
- Discarding or rejecting finished products and raw materials that do not meet approved specifications
- Performing environmental monitoring in the manufacturing facility
- Reporting inspection and testing results with those responsible for products, materials and/or facilities, and recommend necessary corrective actions where necessary
- Maintaining accurate paper and electronic records
- Updating or creating of laboratory procedures if required
- Assisting in non-routine analysis, laboratory investigation, change control, deviation report writing, as well as non-conformance management
- Assisting the development and validation of new lab equipment or test methods
- Developing and maintaining specialized technical expertise in order to provide support for existing products and ongoing GxP operations as required
- Driving continuous improvement projects as required
- Participating in EHS program (e.g. safety inspection) and complying with EHS regulations & policies
The essential requirements of the job include:
- Diploma with reasonable work experience OR equivalent relevant laboratory work experience. Fresh graduates with a degree in Science are welcome to apply
- Extremely detail and accuracy-oriented with good written and verbal communication skills
- Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, and technical writing skills (create and edit procedures)
It would be a plus if you also possess previous experience in:
- Knowledge and experience of a GxP environment or other regulated industry
- Ability to write clear technical documentation
