Regulatory affairs jobs in Leeds

Job Opportunity: Principal Regulatory Writer (Remote) About Us: We are a dynamic and growing medical communications agency committed to excellence in pharmaceutical communications. As we expand our clinical/regulatory department, we are actively seeking a talented and experienced Principal Regula...

Policy Manager UK Professional Membership Body Homebased – Scotland, Northern Ireland or Wales Basic Salary £32,000-35,000 with benefits 27 Days Holiday, 5% Pension, Private Healthcare and L&D Permanent, Full Time Our client a well-respected and reputable UK professional membership body is curren...

Job Title: Senior Medical Director-Neurology/Neuromuscular Location : Remote in Belgium, Netherlands & UK only Salary: Competitive Salary + Shares + Bonus etc Contract Type: Permanent FTE: Full time Company Summary We are currently supporting a growing biotechnology company in Belgium this can be...

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...

Walker Cole International is supporting one of its clients with their search for a Medical Affairs Lead. This is an opportunity to join a growing business with a broad portfolio covering Prescription Medicines (Rx), Cosmetics, Medical Devices and Homecare products. The Medical Affairs Lead is res...

Senior Director of Regulatory Affairs – UK remote. We are looking for a Senior Director of Regulatory Affairs, who will report into the senior leadership team and play a key role for the company strategy & direction by acting as their primary liaison to the EMEA, and wider EEA. Extensive experien...

Initially for 6months at 50%. The role is a Scientific Publication manager at an Associate Director level. Hands-on experience of Leading Scientific Publications for journal and congress submissions, including publication planning and delivery Experience of working in medical affairs in the pharm...

VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS. ...

THIS JOB CAN BE BASED ANYWHERE IN THE EU Company Description PrimeVigilance (part of Ergomed PLC) is a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America an...

Planet Pharma are partnered with a mid-large medical device company who have seen over 55% growth recently and are hoping to implement more in the coming years. Our client is seeking Cath Lab Nurses to become Clinical Application Specialists and join their team in the United Kingdom. The Candidat...

Head of Regulatory Affairs / Regulatory Director Salary : £150,000 - £200,000 per annum Benefits : Plus shares, non-contributory pension, and bonus Location : Remote / Hybrid (depending on your location) Must be UK based. About the Role : We are seeking a highly skilled and experienced Head of Re...

In September 2023, DCC Energy shared its “cleaner energy in your power” strategy with an ambition to double profits and half carbon by 2030. We aim to deepen out the path to net zero emissions for our customers, thanks to a multi-energy product slate and integration capability. Among other initia...

Important Note: UK-Based Candidates and UK Experience Required Novumgen – the group of Entrepreneurs and Scientists. Novumgen is a diverse, integrated specialty pharmaceutical and biological company focused on investing, developing, manufacturing, and supplying innovative products that provide be...

About the Regulatory Affairs Advisor job. Assist and advise members, clients and colleagues on the content, application and interpretation of regulatory requirements as well as the initiation of new business and deliver contract services on time and within budget. Contribute to the development an...

Regulatory Affairs Specialist - Medical Device .We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.As a Senior Reg...

Role: Regional Coordinator Type: Permanent Location: Midlands We currently working with a global pharma who is looking for its next regional Coordinator to come on board within the pharma immunology department. The team is looking for highly organized, detail-oriented candidates who are strong co...

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 Advisor (Arabic 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...

Senior Regulatory Affairs Specialist - Medical Device 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/strategies for new products and changes to exi...

Join the regulatory affairs team at a global pest control products company. CLP, GHS, regulatory affairs, legislation, regulatory support, global regulations, REACH, safety data sheets, biocides, pesticides. ...

This 12-month interim role offers a high degree of autonomy and the flexibility of remote work at a leading pharmaceutical company. About the Role: This is a unique opportunity to jo... ZIPC1_UKTJ

Company: Generis Enterprise Technology Limited Job Title: Training Documentation Specialist (Remote) Location: Remote – UK Contract Status: Full-time / Permanent Staff - 40 hours per week Mon-Fri Salary: Dependent on experience Training Documentation Specialist Overview: The Training Documentatio...

Regulatory Affairs Lead – Remote – Competitive Package BioTalent are exclusively supporting an innovative UK based start up AI-backed software medical device company in their search for an experienced Software as a Medical Device (SaMD) Regulatory Affairs Lead. The company aims to effect large-sc...

NEC has an Immediate Need for the following: Senior UK Nuclear Licensing Engineer (93-011924-04) NEC has an immediate need for an experienced Senior UK Nuclear Licensing Engineer to support a long-term contract. Candidate must have prior UK nuclear licensing experience. This role is remote (95%) ...