Trabajos regulatory affairs en Leeds

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...

Associate Director Regulatory Affairs.Competitive salary + bonus + car allowance + shares/stocks .Reporting to the Vice President of Regulatory Affairs, the .Director of Regulatory Affairs.Focus for oversight includes ensuring appropriate manufacturing and control of drug substances and drug prod...

Planet Pharma is currently recruiting for a Regulatory Associate Manager who specialises in Cosmetics or Skin care working for a single sponser. This position is fully remote anywhere in the UK. Main Job Tasks and Responsibilities: Ensure all cosmetic products comply with EU regulations, includin...

Director Global Regulatory Affairs. The Director, Global Regulatory Affairs will be responsible for developing, implementing and advising on global regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives. ...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...

We are currently seeking a talented Product Developer to join our team. Based in our Leeds head office and reporting directly to the Product Manager, you will play a crucial role in the development of our apparel and tactical products collections.. This is an exciting opportunity to work in a col...

Regulatory Affairs Associate Manager - Cosmetics. Planet Pharma are partnered with a niche mid-sized CRO assisting them with the search for an Associate Manager, Regulatory Affairs to work on an initial 6+ month project with a focus on Cosmetic products. The Associate Manager will ensure products...

Uxbridge or Cambridge – 1 day on-site per month.This role will support one or more products from a regional regulatory perspective.As a member of the Global Regulatory Team (GRT), they will achieve the desired labelling by developing and executing regional regulatory strategies and managing effec...

Regulatory affairs CMC Consultant.Provide advice to clients on quality aspects of drug development and regulatory requirements, in close collaboration with cross-functional experts from the team.Ensure that the content of CMC work-packages and documentation are phase appropriate, meet regulatory ...

We have an opportunity for a Senior Regulatory Manager within the Clinical Development team. Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone regulatory project, with guidance from senior staff as appro...

This role will work a Flex/Hybrid schedule and must be located within a commutable distance of Warsaw, IN, Raynham, MA, or Leeds, UK. About Johnson & Johnson At Johnson & Johnson, we believe health ...

Proclinical is seeking a Director for Global Regulatory Affairs CMC. ...

An opportunity for a Chemical Regulatory Affairs Specialist to join a global chemical trade association as manager of global regulatory intelligence. You will be responsible for: Regulatory horizon scanning Tracking and analysing updates and changes to global chemical regulations Assessing the im...

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...

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...

Reporting to the Chief Regulatory Officer, this role will be responsible for all regulatory activities for medical device and combination products, including defining the device regulatory strategy and overseeing all device submissions across global markets. Device Regulatory Affairs, Senior Dire...

Director, Clinical Research Physician (CNS) Our client is a Biotech company with a focus on neuroscience drug development with early-stage and late-stage clinical studies, now have approval for a Director, Clinical Research Physician role working within the Clinical Science team. This hire will w...

Senior Licensing Engineers support GEH Nuclear Energy Americas LLC Regulatory Affairs in the preparation, review, & delivery of BWRX-300 licensing submittals to clients or directly to the various nuclear regulators & will provide support for license application processes for future customers that...

Senior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist opportunity working for a growing pharmaceutical company that specializing in medicinal, non-medicinal, medical devices, and OTC products. Due to the size of the business, a well versed Regulatory Affairs professional is r...

A lower degree in environmental science, ecotoxicology, environmental toxicology or similar subject Ideally a higher degree (MSc/PhD) or other post graduate qualification. Graduate Environmental Consultancy role in field of chemical regulatory affairs and risk assessment. Degree in Ecotoxicology,...

Regulatory Affairs Consultant, you will have the below responsibilities:. To be considered for the Regulatory Affairs Consultant FTC, you will have the following:. ...

Join the Product Stewardship team at a global high-performance material/chemical business. We are looking for an experienced chemical regulatory generalist who has EU REACH experience, knowledge of similar global schemes and the ability to be able to research issues, work out costs and strategy a...

Professional Support Lawyer - Insurance and Healthcare About the Firm Our client is a distinguished defendant insurance practice, ranked among the Top 40, and recognised as a Legal500 staple. With over 1500 employees across the Midlands and North UK, the firm was awarded Large Law Firm of the Yea...

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...