Regulatory affairs jobs in Glasgow

Senior Regulatory Affairs Associate. As a Senior Regulatory Affairs Associate, you will play a crucial role in ensuring regulatory compliance for our medical devices. ...

Our client, a successful and growing .This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creative solutions in order to obtain approval for initial BLA/NDA as well as post-approvals var...

I am working with a growing pharmaceutical company who provide over-the-counter (OTC) pharmaceutical products dedicated to enhancing the health and well-being of customers.They're currently in the next phase of growth for the company as they're overtaking a consumer portfolio from a huge company ...

Regulatory Affairs Advisor (French Speaking).At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised f...

Regulatory Affairs Specialist - Lifecycle Maintenance.We are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio.The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle na...

Lead Design Engineers and Graduate Engineers within the technical team and be accountable for scheme design, consultancy / feasibility studies, technical standards, regulatory affairs and associated legal processes. The Senior Designer Engineers will have overall responsibility for creating desig...

Regulatory Affairs – Senior CMC Dossier Manager.Contract position until December 2024, inside IR35.CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio.This will be supporting two major projects and will be ...

Create and execute regulatory strategies on a global scale, which involves proactively identifying regulatory risks and exploring various options. Monitors regulatory trends and guidelines, collaborating closely with the Chief Medical Officer to devise optimal regulatory strategies and support ti...

We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, ...

A degree in Science or Engineering. ...

Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device Associate.Main Purpose of Job and Objectives:.Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strateg...

Role: Global Labelling Lead Location: United Kingdom - Remote Salary: Very competitive salary on offer Planet Pharma are supporting a leading global biotech company with the search for a new Global Labelling Lead to join them during an exciting period of growth! Perfect for someone looking to uti...

Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis. Programming is the department that oversees and deli...

Our client is one of the leading global CDMOs, committed to meeting partners’ evolving needs through operational excellence, scientific expertise, and customer connectivity. We are currently seeking a candidate with a robust background in in-licensing to fill this newly created position. The Busi...

The Nudge Group is exclusively working with a dynamic and innovative pharmaceutical company at the forefront of developing cutting-edge solutions to improve public health. Committed to advancing nicotine delivery methods, we are seeking a talented and motivated Product Development expert to add t...

The Company Scendea is a leading product development and regulatory consulting practice serving the pharmaceutical and biotechnology industry. Scendea’s international team offers strategic and operational support in the fields of CMC, nonclinical/toxicology, clinical/medical and regulatory, which...

Medical Science Liaison - UK Are you an outstanding professional, keen to influence product development, and improve patient outcomes through your medical and scientific knowledge? If you're passionate about advancing healthcare and driving positive change, we want you in our team. Join us as Med...

Biostatistician II / Senior Biostatistician – Innovative International Pharma– UK - Hybrid / Fully Remote We have partnered with a renowned global pharma, who are looking for exceptional Biostatisticians ( Entry level to Senior level ) to join their pioneering and innovative team within Global St...

Calling Experienced Specialty Ingredients Recruitment Specialists: Remote Work, Top Pay, Niche Focus! £35k-£45k + 10-20% commission + additional financial incentives enabling you to earn up to 40% of your billings Seeking a move in your specialty ingredients, flavours, fragrances, cosmetics & che...

Company: Generis Enterprise Technology Limited Job Title: Technical Support Analyst / Support and Development Liaison (Remote) Location: Remote – UK Contract Status: Full-time / Permanent Staff About us Generis is a fast growing and successful UK-headquartered developer of world-class Content and...

Title: Clinical Trial Manager - Global Pharma - Complex Trials Location: London Duration: Full Time Salary: Competitive Based on Experience We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. Y...

The candidate must have UK level submission experience. The purpose of the Regulatory Affairs Associate/Senior Associate role is to manage the operational and technical aspects of regulatory affairs for the UK and Ireland marketing affiliate and the Maltese marketing affiliate, including: Execute...

Senior Design Engineer North Lanarkshire £60,000 + £5,400 car allowance Fourblue is working with a leading ICP and EV (electric vehicle) charge point installer. Offering a comprehensive service from planning through to installation and supporting businesses with their net-zero obligations. Carryi...

Role: Regulatory Affairs Role Type: Contract Location: Hampshire Duration: 12 Month We are currently partnered with a global Pharmaceutical company who are now looking for a regulatory affairs associate to execute the Regulatory Plan/objectives to ensure the success of new product registrations f...