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

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