About the role
AI summarisedThis is an entry-level QA Specialist Trainee position at Roche, part of a Train & Place program. The role focuses on maintaining and improving change control systems and processes to ensure GMP compliance in the pharmaceutical industry. The trainee will develop competency in change control, coordinate review and approval of change requests, and support regulatory inspections.
BiopharmaFull-timeGeneral
Key Responsibilities
- Ensure adherence to the Change Control management systems and processes
- Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed
- Evaluate Change Control requests for process, validation, regulatory and product impact
- Coordinate the review and approval process of change requests to ensure timely execution of changes
- Ensure all site major changes are managed appropriately to meet the expectation of the global change control board and meets site project timelines
- Participate in cross functional and cross site change management forums
- Collaborate with departments to ensure change control activities are executed efficiently and effectively, to provide supporting assistance to stakeholders in the process
- Ensure completion of required change control actions prior to lifting lot disposition restrictions
- Assist in the development and delivery of training materials and qualifications for Change Control processes and Change Management applications
- Perform Change Records review in support of Annual Product Review activities
- Ensure maintenance and continuous improvement of change control and processes
- Support regulatory inspections and provide audit support, which may include facility, utility, equipment documentation review
Requirements
- Education: Diploma/Degree in Engineering or Science discipline is preferred
- Fresh graduates/mid-career professionals who are switching out of other industries
- Strong knowledge of Change Control principles, practices and standards for the pharmaceutical industry
- Strong knowledge of cGMP regulations relevant to the pharmaceutical industry
- Systematic, meticulous and analytical approach to evaluation and execution of tasks
- Demonstrate excellent verbal and written communication skills in English