Responsibilities:
- 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
