Quality Control Technician
Description✓Quality Control Technician
✓Liverpool
✓Temporary
✓CDM Life Science are keen to speak with experiences Quality Control Technicians to work for our global pharmaceutical client in Liverpool.
✓Reporting to the Quality Manager, the successful candidate will be tasked with maintaining laboratory and office areas in compliance with EHS and CGMP requirements.
✓* Archive completed laboratory documentation in a timely manner.
✓* Chemical and/or microbial based analyses of purchased and manufactured materials, Utilities/EM, stability samples and non-routine samples
✓Report and approve results using standard laboratory systems ensuring all statistical monitoring charts [paper and electronic] are updated in a timely manner.
✓* Perform all aspects of sample handling e.g sample receipt, storage and disposal as per procedures.
✓* To follow Standard Operating Procedures [SOPs] and best practice guidance.
✓* Document activities and observations in reports.
✓* Review and verify the work of fellow scientists to ensure correct procedures have been followed.
✓The successful candidate will have,
✓* 3-5 years’ experience in a GMP environment.
✓* BSc or higher in a Chemistry-related subject, or comparable laboratory experience.
✓* Experience of report and protocol writing would be highly advantageous
✓* Have excellent communication skills and an ability to build strong working relationships
✓* Ability to translate technical concepts Show more →
✓Liverpool
✓Temporary
✓CDM Life Science are keen to speak with experiences Quality Control Technicians to work for our global pharmaceutical client in Liverpool.
✓Reporting to the Quality Manager, the successful candidate will be tasked with maintaining laboratory and office areas in compliance with EHS and CGMP requirements.
✓* Archive completed laboratory documentation in a timely manner.
✓* Chemical and/or microbial based analyses of purchased and manufactured materials, Utilities/EM, stability samples and non-routine samples
✓Report and approve results using standard laboratory systems ensuring all statistical monitoring charts [paper and electronic] are updated in a timely manner.
✓* Perform all aspects of sample handling e.g sample receipt, storage and disposal as per procedures.
✓* To follow Standard Operating Procedures [SOPs] and best practice guidance.
✓* Document activities and observations in reports.
✓* Review and verify the work of fellow scientists to ensure correct procedures have been followed.
✓The successful candidate will have,
✓* 3-5 years’ experience in a GMP environment.
✓* BSc or higher in a Chemistry-related subject, or comparable laboratory experience.
✓* Experience of report and protocol writing would be highly advantageous
✓* Have excellent communication skills and an ability to build strong working relationships
✓* Ability to translate technical concepts Show more →