GMP Production Operative
- Recruiter
- Confidential
- Location
- Loughborough
- Salary
- Competitive
- Posted
- 23 Jul 2022
- Closes
- 20 Aug 2022
- Sectors
- Health, Nursing & Social Care
- Contract Type
- Temporary
- Hours
- Full Time
Excellent Medical Device company based in Loughborough are looking for a number of GMP Production Operatives to join them.
Reporting to the Production Supervisors, the GMP Production Operatives, will be producing Medical Devices, to very high quality standards, working with a small team of other technicians and process operatives.
Main responsibilities include:-
Undertake manufacturing tasks following instructions and Standard Operating Procedures.
Work safely within technical areas, maintaining excellent housekeeping and always adhering to HSE and quality management systems.
Support the validation and verification testing of product and equipment; ensuring that requirements of the Quality Management System have been met.
Report any HSE matters and identified opportunities for improvement to supervisors/management.
Complete required paperwork.
Operation & maintenance of production equipment and machinery.
Understand the importance of working to high standards to ensure that regulatory and compliance requirements for ISO 9001, ISO 13485 and other international regulatory requirements are achieved.
We are looking for people who have worked in production previously, ideally with experience working within a GMP Pharmaceutical environment, with excellent attention to detail.
This is a fantastic opportunity to join a company with ambitious growth plans and become part of the team
Reporting to the Production Supervisors, the GMP Production Operatives, will be producing Medical Devices, to very high quality standards, working with a small team of other technicians and process operatives.
Main responsibilities include:-
Undertake manufacturing tasks following instructions and Standard Operating Procedures.
Work safely within technical areas, maintaining excellent housekeeping and always adhering to HSE and quality management systems.
Support the validation and verification testing of product and equipment; ensuring that requirements of the Quality Management System have been met.
Report any HSE matters and identified opportunities for improvement to supervisors/management.
Complete required paperwork.
Operation & maintenance of production equipment and machinery.
Understand the importance of working to high standards to ensure that regulatory and compliance requirements for ISO 9001, ISO 13485 and other international regulatory requirements are achieved.
We are looking for people who have worked in production previously, ideally with experience working within a GMP Pharmaceutical environment, with excellent attention to detail.
This is a fantastic opportunity to join a company with ambitious growth plans and become part of the team