Gi Group
12 Feb 2019
12 Mar 2019
Contract Type
Full Time

Elstree, Herts
Permanent role
9-5.30 Monday-Thursday 9-5 Friday

Working with one of the world's leading medical technology companies offering innovative products and services in Orthopaedics, Medical and Surgical equipment. Reporting directly to the Logistics & Customs Team Leader.

Main purpose of role
To ensure the effective running of the cleanroom to meet all implant delivery requirements whilst remaining quality and regulatory compliant.

Key tasks
Organise and maintain Cleanroom as required by the Quality Procedures.
Maintain high degree of cleanliness and contamination control throughout the cleanroom and changing area.
To follow good clean room practices
Ensure compliance with all standard operating procedures and work instructions
Maintain a high level of attention to detail.
Obtain monitoring samples under controlled condition for process verification.
To maintain minimum stock levels of all materials required for the effective operation of all clean room activities.
Maintain equipment in working order by regular service and keep records as required by the Quality Procedures.
Handle, store and dispose of all cleaning and other chemicals as controlled by the COSHH regulations.
Etch serial numbers wherever required.
Thoroughly clean all components and place them in sealed bags as required by the Quality Procedures.
Ensure components that are to be gamma irradiation sterilised are packed and labelled according to the requirements.
For cleaning and packaging ensure that the work completed is identified by your signature and date on the appropriate documentation.
Any other tasks that sits outside your current role from time to time to support the activities of the business.

Qualifications, skills and desirable experience
No formal qualifications required but experience of working within a regulated environment preferred.

Special features
Our client operates under strict Quality procedures and where these relate to your role you should aim to achieve the required levels of conformity as necessary. This will ensure that you are fully aware that any non-compliance or improper performance of your role may occur in a defective device. You also should need to ensure that you remain up to date with the contents of the Quality manual and how this affects your duties.

If you are interested and feel you have relevant experience then please contact Rosie Carden for a confidential discussion on .

Gi Group Pharmaceuticals provides a tailored Account Managed Service and dedicated Pharmaceutical recruitment team and partners with many different Pharmaceutical and Biotechnology clients throughout the globe and the United Kingdom.

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