Regulatory affairs jobs in Stevenage

Implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements and manage the development of the regional product label by collaborating with the Labeling Working Group. Participate in core re...

Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development ...

Senior Manager Regulatory Affairs Writing A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. The role will play a pivotal role in the ...

Regulatory Affairs Specialist - Fully Remote This is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The successful ...

Responsibilities · Responsible for maintaining and supporting the promotion of regulatory affairs and ensuring that overall regulatory compliance of the Company, is maintained. · The position ...

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 ...

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 ...

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 ...

Professional Standards Coordinator, Professional standards Manager, Scientific Ethics, Regulatory Affairs, SOPs, Process improvement, Risk Management, MRSC, Project Management, Best practice etc REF ...

Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.

A thorough understanding of global drug development functional areas including preclinical, clinical, regulatory affairs and manufacturing * Highly collaborative, strong relationship building skills ...

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 ...

As the Product Safety Assistant you will have: * • Experience in a Regulatory Affairs or an R&D role where regulatory compliance was part of regular duties • Experience within the chemicals or ...

... Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.

... Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors.

... Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors.

... Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors.

... Corporate Affairs, and Sales and Marketing, our approach is focused on driving the improved ... regulatory upheaval. We've proudly stood beside the institutions and businesses which make the UK ...

Associate Director (Regulatory Affairs). As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory Affairs. Title: Associate Director (Regulatory Affairs). Lead an...

Job title: Senior Regulatory Affairs Manager CMC. A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. CMC Regulatory Affairs within the pharmaceutical or biotechnology industry. The role will be responsible for the development, executio...

As a Senior Regulatory Affairs Associate, you will play a crucial role in ensuring regulatory compliance for our medical devices. You will collaborate closely with the Regulatory Affairs Manager and cross-functional teams to prepare and review regulatory submissions, manage design dossiers, and f...

Determining and/or validating existing regulatory information including legal ingredient declarations, allergen information, nutritional, analytical tolerances, suitability based on product composition in our online formulation repositories. Preventing any successful challenge to our products, pa...