About the role
AI summarisedQC Chemist I at Thermo Fisher Scientific, a biotech/pharma company, performing quality control testing of raw materials, in-process samples, and finished products using analytical techniques under cGMP conditions. The role involves documentation, equipment maintenance, investigations, and continuous improvement in a 12-hour shift environment.
Life SciencesFull-timeGeneral
Key Responsibilities
- To 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.
- To perform and coordinate monitoring, calibration, and maintenance of laboratory equipment.
- To lead the preparation of technical documentations such as protocols, position papers and risks assessments.
- To perform write up for laboratory investigations, deviation and on time closure in line with Quality Management system procedures. (if required)
- To support method transfer/verification/validation for new product introduction.
- To perform periodic reviews for laboratory documents.
- To manage QC chemicals and consumables inventory stock check.
- To maintain the accuracy, completeness, and compliance of laboratory data.
- To participate in continuous improvement activities.
- To maintain own training records.
- To communicate effectively with others on site and internationally and to participate with them in problem solving activities.
- To 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.