An established UKAS accredited Biotechnology organisation with a variety of analytical testing services, have an opportunity for a Quality Specialist to join the team.
Reporting into the Quality Manager, the Quality Specialist will be responsible for the generation and progression of Quality Systems including NCFs, INVs, CAPA, change controls and process improvements.
As part of this role, you will support the implementation and monitoring of the quality management system in compliance with cGMP and company policies within the facility.
You will also support equipment maintenance and calibration practises, and ensure all validation activities for all critical equipment are conducted to GMP standards
To be considered, you will have a minimum of a degree (or equivalent) in a Life Science with experience of maintaining quality standards experience in a GMP environment.
Quality Assurance experience in Biotechnology or a similar field is preferred.
You will also have:
Knowledge of cGMP and regulations.
Ability to work inter-departmentally and with customers.
Demonstrate ability for effective planning, organizing, and controlling proficiency.
Good ability to complete assignments under timelines and work under pressure