About the role
Intern - Validation Engineering role based on the published job description. Key responsibilities and requirements were extracted directly from the posting for quick review.
BiopharmaOnsite
Key Responsibilities
- Support the day-to-day operation of approved Validation SOPs / Plan / Policies for a multi-platform, multi-product, GMP biotech contract manufacturing facility, if assigned.
- Develop Validation Protocols and Reports including supporting validation discrepancies and deviations investigation / closure, if assigned.
- Support the execution of validation activities with respect to cleaning, facilities/equipment and computerized system stated in validation plan/ protocol and ensure these are carried out in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion.
- Participate actively in investigations or troubleshooting discrepancies/ deviation encountered during commissioning and qualification.
Requirements
- Pursuing a Degree in Life Sciences or Engineering discipline or equivalent Demonstrates good oral and written communication skills in English Meticulous and Systematic Ability to adapt to rapidly changing priorities and the flexibility to support operations in accordance with the manufacturing schedule Must be highly motivated, able to work independently as well as a Team player, with strong focus on Safety, Quality and timeline.
- Willing to work at Singapore Tuas Bay Link .
- Able to commit full time intern from Monday to Friday.