- Sengkang North-east Region (Singapore) Singapore
Working Location
Job Description
Responsibilities
Role Overvie
w:This contractual role focuses on leading the transfer and optimization of purification processes for cell culture manufacturing within a biopharmaceutical production facility. The position requires hands-on technical leadership to ensure seamless technology transfer from customer or donor sites to the Singapore facility while maintaining compliance and operational excellence. Your work will directly impact the successful execution of purification stages, ensuring reliable and scalable manufacturing outcomes for global client
s.
Key Responsibiliti
es:• Lead the timely and successful transfer of purification processes of customer manufacturing into the production facility, coordinating with MSAT team members, customer technical experts, manufacturing, quality assurance, and quality contr
ol.• Prepare, execute, monitor, and complete post-campaign activities for purification processes, ensuring adherence to technical and regulatory standards while supporting facility proficien
cy.• Monitor processes regularly to identify behaviors and trends, prospectively flagging issues and leading cross-functional investigations into deviations involving multiple departments and custome
rs.• Review purification process manufacturing batch records, provide technical input to document specialists, and identify training needs for manufacturing operato
rs.• Support plant start-up, pilot runs, and commercial operations by troubleshooting process excursions, authoring technical reports, and driving change requests to implementati
on.
Required Skills & Qualificati
ons:• Bachelor’s degree or higher in Chemical Engineering, Biotechnology, Biochemical Engineering, or related field, with a minimum of 5 years of relevant experience in bioprocess purification or MSAT ro
les.• Demonstrated experience in technology transfer of purification processes within biopharmaceutical manufacturing environme
nts.• Strong technical writing skills with proven ability to review and contribute to batch records, technical reports, and change control documentat
ion.• Experience leading cross-functional investigations and process troubleshooting in GMP-regulated environme
nts.• Familiarity with cell culture or purification unit operations, process monitoring tools, and regulatory compliance in biomanufactur
ing.
More About the Opportu
nity:This role operates within a global biomanufacturing leader’s Singapore facility, supporting end-to-end purification process integration for high-value client projects. You will have the opportunity to deepen expertise across multiple purification platforms while contributing to scalable, compliant bioprocess operations. The position offers exposure to international technology transfers and collaboration with technical experts across multiple s
ites.
Equal Opportunity Emp
loyer:We hire based on skills and expertise. All qualified candidates are welcome regardless of background, experience, or prior employment history. Applications are reviewed solely on demonstrated technical ability and qualifica
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