About the role
AI summarisedThis is a 15-month structured on-the-job training program (Career Conversion Programme - Attach-and-Train) designed to build the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry. This role offers intensive training within GSK's manufacturing environment.
BiopharmaOnsiteQuality
Key Responsibilities
- Ensure all data supporting analytical methods are accurate and take correct action to address any issues.
- Contribute to plans for implementing new testing technologies and methods.
- Assess changes in analytical assessments that may impact product quality, validation, or cGMP compliance.
- Lead or participate in investigations arising from laboratory incidents and recommend remedial actions.
- Draft, review, and update essential laboratory documents including testing protocols, procedures, analytical methods, and guidelines related to GMP.
- Ensure all manufacturing raw materials, non-routine samples, and products are analyzed according to stipulated quality requirements.
- Stay updated with pharmacopeial and other health agency guidelines.
Requirements
- At least a Degree in Chemistry or a relevant science.
- Must be a Singapore Citizen or Permanent Resident.
- Ability to organize work and handle multiple priorities while meeting deadlines.
- Basic statistical mathematical skills.
- Ability to work effectively in a diverse team.
- Understanding and adherence to applicable safety requirements.