- Islandwide (Singapore) Singapore

Working Location
Job Description
Responsibilities
Responsibilities :
· Understand and comply with company’s policies,particular in IP (Intellectual Protection).
· Ensure the compliance with EHS requirements indaily work.
· Draft gap analysis, risk assessment, technologytransfer protocol and process flow diagram for new transfer project.
· Lead gap analysis, risk assessment, changecontrol and technology transfer protocol for cross-site late stage project.
· Lead the process validation activities, includingchange controls, process control strategy, PPQ/supportive study protocols, defineand identify CQA/CPPs, be trainers, CPV campaign, comparability study etc.
· Working with the cross functions and determinethe details of technology transfer and solve related problems
· Responsible for establishing and maintaining theknowledge platform for technology transfer.
· Support the optimization of DP manufacturingprocess.
· Support technology transfer relateddocumentation management.
· Support the investigation of deviations duringtechnology transfer.
Requirements:
· Bachelor degree or above, major in Microbiology,Chemistry, Biotechnology, Biochemistry, Pharmacy or other appropriateeducation. 5 years+ work experience.
· Be familiar with basic knowledge of asepticassurance and GMP regulation. Understand DP process development and asepticfilling. At least three years’ experience in biopharmaceutical industry, someknowledge of drug product formulation, process scale-down and -up, and processcharacterization is preferred.
· Team player with good organization andcommunication skills.
· Pro-active, high sense of responsibility,self-discipline, focus on details and result oriented.
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