About the role
AI summarisedThe QC Chemist I role at Thermo Fisher Scientific involves performing quality control testing on raw materials, in-process samples, and finished products under cGMP conditions. The position supports product quality and reliability through analytical testing, documentation, equipment maintenance, and participation in continuous improvement initiatives. This role requires working in a regulated laboratory environment with opportunities for professional growth and collaboration across teams.
Life SciencesOnsite
Key Responsibilities
- Perform QC testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies
- Perform and coordinate monitoring, calibration, and maintenance of laboratory equipment
- Lead the preparation of technical documentations such as protocols, position papers and risks assessments
- Perform write up for laboratory investigations, deviation and on time closure in line with Quality Management system procedures
- Support method transfer/verification/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
- Participate in continuous improvement activities
- Communicate effectively with others on site and internationally and participate with them in problem solving activities
- Ensure cGMP is applied and adhered to in their area 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
- Excellent organizational skills
- Strong in analytical skill and problem-solving skills
- Degree in Chemistry or strongly related scientific discipline
- At least 2-3 years relevant industrial experience
- Ability to apply GMP regulations and other international guidelines to all aspects of the position