An interesting new instruction for an established client specialising in the manufacture of fast moving consumer goods. The Position: Research & Development Administrator/Co-ordinator. Employment Type: Full-time 37 hours a week, Ongoing temporary contract – Hybrid working (Office days Tuesday & Wednesday Commencement: the successful must be able to commit to a start date in August 2025 The ideal person: The role is considered ideal for a really strong administrator who enjoys working in a fast paced environment where no two days will be the same • Outstanding attention to detail is paramount • Proficiency with MS Office • The ability to work to deadlines • Excellent communication skills (written and oral) • A friendly team player and a can do approach • Any previous experience gained within a manufacturing setting could be helpful Key Job Role: The R & D Administrator/Co-ordinator will be involved in the creation and approval of specifications for certain brands, so gathering lots of key information from your colleagues and adding this technical info

An interesting new instruction for an established client specialising in the manufacture of fast moving consumer goods. The Position: Research & Development Administrator/Co-ordinator. Employment Type: Full-time 37 hours a week, Ongoing temporary contract – Hybrid working (Office days Tuesday & Wednesday Commencement: the successful must be able to commit to a start date in August 2025

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