Responsibilities:
- Support the tech transfer into the facility
- Coordinating with Manufacturing, Process Development, Supply Chain, Planning, Facilities and Engineering, as well as Quality to introduce new Drug Substance products using project management tools (i.e. Smartsheet).
- Biologics drug substance technical knowledge who participates in projects, including aiding in commissioning and qualification and aiding in training staff on equipment and processes
- Owns New Product Introduction Change Controls and collaborates with partners to drive accurate completion.
- Ensures that manufacturing production documents (e.g. Standard Operating Procedures) are accurate and up to date.
About You:
- Project management and meeting facilitation
- Technical writing skills
- Experience in GMP manufacturing operations
- Strong technical knowledge of drug substance processing and a broad understanding of related disciplinary areas in bioprocessing.
- Ability to communicate sophisticated technical information with internal and external colleagues in both presentation and technical writing forms
Based in Tuas.
1 year contract. Option to extend/annual renewal depending on performance
