About the role
AI summarisedSix-month biopharma engineering internship in Singapore focused on global compliance, automation, and digitalization projects. Interns lead improvement initiatives on GMP materials, PFAS and extractables/leachables compliance, and develop dashboards using Power Platform/BI while collaborating with multidisciplinary teams across GSK sites.
BiopharmaOnsiteEngineering
Key Responsibilities
- Lead to drive improvement in standards and compliance across the GSK site network with respect to International and local regulation, GSK recognized standards & industry best practices
- Support to develop and deliver strategies for Engineering Product contact materials within manufacturing supply chain of sites
- Work on critical projects related to Environmental Regulatory compliance (such as PFAS) and Quality Regulatory compliance (Such as Extractable & Leachable)
- Demonstrate creative mindset on designing solutions through academic research and benchmarking industry best practices to improve the Safety and Quality compliance
- Explore opportunities in digitalization space (MS Power Platform, BI or other dashboarding tools) to enhance optimization and visualization of business and process data
- Lead research and data analysis to support project decision-making
- Assist in tracking project progress and identify potential risks and issues
- Assist in preparing reports and presentations on project status and performance
Requirements
- A keen interest in Manufacturing and Engineering world of biopharma industry
- Strong analytical and troubleshooting/problem solving skills
- Competency in data research, analysis, and interpretation of results
- Excellent communication and interpersonal skills with brilliant English proficiency
- Ability to work independently and as part of a team
- Technical competency in Engineering and Material Science
- Enjoy working and collaboration cross-functionally and across global teams