About the role
AI summarisedThis 15-month talent development programme is designed to build the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry. The role involves ensuring quality compliance standards are defined, established, and maintained on-site in accordance with internal and external regulatory expectations regarding current Good Manufacturing Practices (cGMP). This programme is exclusively for Singapore Citizens and Permanent Residents.
BiopharmaOnsiteQuality
Key Responsibilities
- Establish and maintain quality compliance standards consistent with the Quality Management System (QMS) by reviewing site policies, procedures, and training materials.
- Provide advisory support to the business on compliance matters within the quality system.
- Offer QA consultation to stakeholders to resolve issues related to Document and Data Management.
- Manage quality-related Key Performance Indicators (KPIs), including data collation, metric reporting, and identifying opportunities for site quality improvement.
- Ensure the effective implementation of GMP and Data Integrity training.
- Steer and/or implement compliance initiatives and standardization across key quality systems and quality improvement projects.
Requirements
- Graduated with a Bachelor's Degree in a relevant science discipline.
- Must be a Singapore Citizen or Singapore Permanent Resident.
- Good knowledge of quality and manufacturing processes.
- Strong oral and written communication skills.
- Analytical thinking abilities.
- Integrity and a strong eye for detail.