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 hygienically lean environment, so if you would like to work within a supportive team setting on a PERMANENT BASIS, receive on the job training and support 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 downs Readi

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 hygienically

This position is ideal for a good all-rounder and is presented on a long term temporary basis, for around 6 months with the possibility of extension. We are searching for someone personable and reliable who is able to take responsibility for all Data Analytics and administration with a focus on training and development of personnel within the Quality department Excellent organisation skills Able to prioritise effectively Good attention to detail Experience with CAPA beneficial but not essential Advanced understanding of MS Excel Hours; 37 per week (9am-5pm Mon-Thurs, 9-4:30 Fri) with 45 min lunch break (30 mins unpaid, 15 paid) Free parking Free products at the discretion of the client If you have the skills, knowledge and experience we are seeking and potentially available to start asap, then we very much welcome your application. Recruitment Solutions (Folkestone) Limited acts as an employment agency for permanent recruitment and as an employment business for the supply of temporary workers. By applying for this job, you accept the Terms & Conditions, Pr

This position is ideal for a good all-rounder and is presented on a long term temporary basis, for around 6 months with the possibility of extension. We are searching for someone personable and reliable who is able to take responsibility for all Data Analytics and administration with a focus on training and development of personnel within the Quality department Excellent organisation skills

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