About the role
AI summarised15-month trainee role within GSK’s biopharmaceutical manufacturing site in Singapore, focused on quality systems and data integrity. The trainee ensures cGMP compliance, supports QMS maintenance, manages quality KPIs, and drives continuous improvement initiatives.
BiopharmaOnsiteQuality
Key Responsibilities
- Establish/maintain quality compliance standards consistent with Quality Management System (QMS) by providing support in areas such as: Reviewing site policies, procedures and training materials related to quality system
- Providing advisory support to business on compliance area
- Provide QA consultation with stakeholders to resolve issues on Document and Data Management
- Manage quality related Key Performance Indicator (KPI), including data collation, regular KPI metrics reporting and identification of issues and opportunities for improvements in site quality performance
- Ensure the effective implementation of the GMP and Data Integrity training
- Steer and/or implement compliance initiatives, standardization of quality systems across key quality systems and quality improvement projects
Requirements
- Graduated with a Bachelor's Degree in a relevant science discipline
- Relevant experience in the pharmaceutical industry is a bonus
- Preferably with experience in Quality functions
- Good knowledge of quality and manufacturing process
- Good interpersonal and influential skills
- Good oral and written communication skills
- Growth mindset
- Project Management skill
- Analytical thinking
- Eye for details