Support new product introduction (NPI) and technology transfer activities
Support process validation and characterization studies.
Develop process validation and process characterization study protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely manner or in accordance to project timelines.
Manage the execution of process validation and characterization studies and associated deviation root cause analysis (RCA) and investigations.
Collaborate with cross-functional teams to arrange, plan and ensure smooth running and execution of the process validation activities.
Lead / support relevant process and technical change management, and change implementation activities.
Support any other tasks as assigned by the supervisor.
About You:
8-10 years of relevant working experience in the Pharmaceutical/Biologics manufacturing industry with experience in process validation is preferred.
Candidate with Downstream equipment experience will have an advantage.
Compliance with and safety regulations cGMP
Willing to work in Tuas
Duration: 1 year contract role
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