About the role
AI summarisedJoin the Quality Control team at Thermo Fisher Scientific to ensure product quality and reliability through rigorous testing and analysis. This role involves conducting QC testing on raw materials, in-process samples, and finished products under cGMP conditions to support the development of innovative therapeutic products.
Life SciencesOnsite
Key Responsibilities
- Perform QC testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or stability studies.
- Perform and coordinate monitoring, calibration, and maintenance of laboratory equipment.
- Lead the preparation of technical documentations such as protocols, position papers, and risk assessments.
- Write up laboratory investigations, deviations, and ensure on-time closure in line with Quality Management system procedures.
- Support method transfer, verification, and validation for new product introduction.
- Perform periodic reviews for laboratory documents.
- Manage QC chemicals and consumables inventory stock check.
- Maintain the accuracy, completeness, and compliance of laboratory data.
- Ensure cGMP is applied and adhered to in all areas of work.
Requirements
- Ability to work independently and adhere to critical timelines.
- Effective communication skills at all internal and external levels.
- Excellent attention to detail.
- Strong analytical skill and problem-solving skills.
- Ability to apply GMP regulations and other international guidelines.
- Willingness to support shift work (if necessary).