Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Contribute to the development of operation protocols for upstream or downstream operations starting from the dispensary of raw materials up to end of manufacturing process
- Lead and execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for Production
- Support Change Records Assessment and GMP documentation Review
- Responsible for providing support to the assigned manufacturing operations by developing, coordinating and executing small to medium sized projects to ensure planned, predictable production operations in compliance with GMP regulations
- Lead and execute Continuous Process Improvements, CAPAs and Change Records in assigned area
- Provide routine and ad hoc support for planning, coordinating, execution, and performance improvement of key manufacturing processes such as product change over
- Lead project teams to troubleshoot medium to complex problems and support continuous process improvement. Facilitate root cause analysis (RCA) with input from SMEs, develop and implement change to improve performance
- Collaborate with multidisciplinary teams to achieve project objectives
- Assist in experimental design and troubleshooting as needed
- Perform a final clean-up and check of the work area
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
- Bachelor’s Degree in Biomedical Engineering, Biotechnology, Science or equivalent
- Adherence to safety protocols and regulatory compliance
- Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
- Excellent communication skills, both written and verbal, in English
- Experience in Upstream or Downstream GMP environment is preferred
