We are recruiting for a PERMANENT PRODUCTION OPERATOR for an established manufacturing client in the area with an impressive manufacturing site, where they have a number of high speed, high tech, production lines manufacturing their portfolio of products. The role is with a great employer where employee welfare is at the heart of everything they do. You will be working within a hygie ically clean environment, so if  you would like to work within a supportive team setting on a PERMANENT BASIS, receive on the job training and become an integral part of their manufacturing team, we welcome your application. Job Content: The purpose of a Production Operator is to ensure the production lines run efficiently and effectively, ensuring any problems are rectified quickly and ensure that good manufacturing checks are completed, so operating and monitoring their high tech machinery. Ordering and loading components from stores to enable production flow Completing line start up checks Operating and monitoring machines Dealing with product changeovers and wash d

We are recruiting for a PERMANENT PRODUCTION OPERATOR for an established manufacturing client in the area with an impressive manufacturing site, where they have a number of high speed, high tech, production lines manufacturing their portfolio of products. The role is with a great employer where employee welfare is at the heart of everything they do. You will be working within a hygie

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys em improvements to existing processes, to develop and execute process system validations and provides manufacturing quality into to Product Development groups. The role carries responsibility to comply with and promote compliance with the relevant GMP and hygiene procedures and standards in the activities they undertake within the facilities. Education & Experience we are seeking: University degree in a related field of Science or Engineering A professional with technical experience and a demonstrated track record Ideal Skills & Attributes we are seeking: Broad experience of all key areas of Quality Assurance Working knowledge of the MDD, MDR, 21CFR 820, ISO 13485, ISO 14971, I

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys em improvements to existing processes, to develop and execute process system validations and provides manufacturing quality into to Product Development groups. The role carries responsibility to comply with and promote compliance with the relevant GMP and hygiene procedures and standards in the activities they undertake within the facilities. Education & Experience we are seeking: University degree in a related field of Science or Engineering A professional with technical experience and a demonstrated track record Ideal Skills & Attributes we are seeking: Broad experience of all key areas of Quality Assurance Working knowledge of the MDD, MDR, 21CFR 820, ISO 13485, ISO 14971, I

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys

Applications are invited in relation to new vacancy for a SITE SERVICE ENGINEER which is presented on a temporary basis to cover long term sickness. The position is with a key employer and global manufacturing organisation in the area where employee welfare is at the heart of everything they do. The Site Service Engineer reports to the Facilities Engineering Supervisor and there are 2 other olleagues within the Team. Monday to Friday 39 hours per week Excellent rate of pay Snapshot of the role and key experience we are seeking: Applicants from an electrical or mechanical background would be preferred Full driving licence Must be fit and able to manual handle for example 15KG BOAS trained would be helpful Below gives you an example of some of the PPMs you will be required to complete, so a good level of autonomy and trust is required: Checks on Company Vehicles-4W Compressor Condensers-2W Conduct Monthly Meter Readings-1M House Legionella Ctrl Flush-1W Hse Shower Head/Tap Descale-12W Deluge System Test-12W Emergency Shower Test-1W LEV Clean & Inspect-1W L

Applications are invited in relation to new vacancy for a SITE SERVICE ENGINEER which is presented on a temporary basis to cover long term sickness. The position is with a key employer and global manufacturing organisation in the area where employee welfare is at the heart of everything they do. The Site Service Engineer reports to the Facilities Engineering Supervisor and there are 2 other

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys em improvements to existing processes, to develop and execute process system validations and provides manufacturing quality into to Product Development groups. The role carries responsibility to comply with and promote compliance with the relevant GMP and hygiene procedures and standards in the activities they undertake within the facilities. Education & Experience we are seeking: University degree in a related field of Science or Engineering A professional with technical experience and a demonstrated track record Ideal Skills & Attributes we are seeking: Broad experience of all key areas of Quality Assurance Working knowledge of the MDD, MDR, 21CFR 820, ISO 13485, ISO 14971, I

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys em improvements to existing processes, to develop and execute process system validations and provides manufacturing quality into to Product Development groups. The role carries responsibility to comply with and promote compliance with the relevant GMP and hygiene procedures and standards in the activities they undertake within the facilities. Education & Experience we are seeking: University degree in a related field of Science or Engineering A professional with technical experience and a demonstrated track record Ideal Skills & Attributes we are seeking: Broad experience of all key areas of Quality Assurance Working knowledge of the MDD, MDR, 21CFR 820, ISO 13485, ISO 14971, I

A new instruction for a Validation Specialist with an established manufacturing client in the area. This is an exciting opportunity to join the Quality Team on a long term temporary basis for initially 6 months, with the possibility of an extension, and reports to the Validation Lead. The Main Responsibilities: Will be to work with colleagues in the Validation Team on Quality Management sys

We are recruiting for a PERMANENT PRODUCTION OPERATOR for an established manufacturing client in the area with an impressive manufacturing site, where they have a number of high speed, high tech, production lines manufacturing their portfolio of products. The role is with a great employer where employee welfare is at the heart of everything they do. You will be working within a hygie ically clean environment, so if  you would like to work within a supportive team setting on a PERMANENT BASIS, receive on the job training and become an integral part of their manufacturing team, we welcome your application. Job Content: The purpose of a Production Operator is to ensure the production lines run efficiently and effectively, ensuring any problems are rectified quickly and ensure that good manufacturing checks are completed, so operating and monitoring their high tech machinery. Ordering and loading components from stores to enable production flow Completing line start up checks Operating and monitoring machines Dealing with product changeovers and wash d

We are recruiting for a PERMANENT PRODUCTION OPERATOR for an established manufacturing client in the area with an impressive manufacturing site, where they have a number of high speed, high tech, production lines manufacturing their portfolio of products. The role is with a great employer where employee welfare is at the heart of everything they do. You will be working within a hygie