Regulatory affairs jobs in Luton

Quality Assurance and Regulatory Affairs Assistant Full-time position, Monday to Friday, 37.5 hours per week Salary is negotiable depending on qualifications and experience Facility is situated in ...

Quality Assurance and Regulatory Affairs Assistant Full-time position, Monday to Friday, 37.5 hours per week Salary is negotiable depending on qualifications and experience Facility is situated in ...

Quality Assurance and Regulatory Affairs Assistant Full-time position, Monday to Friday, 37.5 hours per week Salary is negotiable depending on qualifications and experience Facility is situated in ...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking ...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary ...

Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management. * Well versed with UK ASA, CAP, BCAP ...

PE Global is recruiting a Regulatory Affairs Manager (CTA) for our multinational pharmaceutical client based in Uxbridge. The role is hybrid and an initial 12-month contract. Responsibilities of the ...

!*Regulatory Affairs Manager - Remote/hybrid in Uxbridge - Global Biotech*! Location: Hybrid in Uxbridge (Can be homebased but will need to attend office when required) Length: 12 month contract ...

We are recruiting for a Regulatory Affairs Manager - EU. The role reports to Director of Regulatory Affairs and is based in our offices near High Wycombe managing a small team. This role is ...

Are you a Regulatory Affairs Manager with Food & Beverage industry experience looking for a new opportunity and to join a growing and exciting organisation? Our client based in High Wycombe are a ...

Who are we? Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across ...

Determining and/or validating existing regulatory information including legal ingredient declarations, allergen information, nutritional, analytical tolerances, suitability based on product ...

Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing ...

Bachelor of Science degree in food science, chemistry or related field or equivalent qualification. * 2-3 years' experience in regulatory affairs within the food industry. * Strong communication ...

You'll get to learn about evolving regulatory requirements and you will be able to confidently support the Regulatory Affairs & Homologation Specialist with the ongoing administration that surrounds ...

Develop, implement and manage our public affairs strategy, leading on public affairs activities ... Manage our horizon scanning and monitoring of the political, legislative and regulatory landscape ...

Develops timelines for submissions under the direction of senior regulatory affairs staff. Provides solutions to extreme complex problems in which data analysis requires an evaluation of intangible ...

Regulatory Affairs : Address regulatory issues promptly and thoroughly, ensuring compliance with all relevant regulations. General Requirements: * Excellent communication skills, both verbal and ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Hobson Prior is seeking a Principal Clinical Consultant with a strong background in clinical development and regulatory affairs. This role will involve providing strategic, technical, and regulatory ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Administer regulatory affairs and conduct full investigations of incidents within strict timeframes. Qualifications and Experience: * Bachelor's degree in Biomedical Science or similar field

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...