Senior regulatory affairs associate jobs in Slough, United Kingdom

Regulatory Affairs Specialist is responsible for leading global regulatory and safety strategy for Air Care products. The role involves representing the Regulatory function in cross-functional teams, overseeing global registration and notification processes, partnering with count ...

A regulatory affairs specialist to join their technical & quality team with a commitment to technical excellence and customer satisfaction. · Manage customer requests related to regulatory documentation for manufactured products. · Support the Sales and Customer Care teams in add ...

This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe.The role involves strategic input into development programs, preparation and submission of regulatory documentation, and post-approval lifecycle manag ...

Job Summary · Sr Manager Regulatory Affairs CMC supports regulatory activities for specialty pharmaceutical products across Europe. · This role involves strategic input into development programs, preparation of regulatory documentation, lifecycle management and due diligence revi ...

This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. · Lead regulatory strategy development for new and existing products. · Review non-clinical and clinical data packages for regulatory adequacy. · ...

This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. · Lead regulatory strategy development for new and existing products. · Review non-clinical and clinical data packages. · ...

If you feel like you're part of something bigger, it's because you are. At Amgen our shared mission—to serve patients—drives all that we do. · ...

SRG are looking for a regulatory affairs submission associate for a pharmaceutical company based in maidenhead. · You will be responsible for establishing and maintaining submission content planners and associated timelines, facilitates tactical submission team meetings, prepares ...

+SRG are looking for a regulatory affairs submission associate for a pharmaceutical company based in maidenhead. · +Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high quali ...

The Senior Associate, Regulatory Affairs will be responsible for administration, maintenance, and business support of Alnylam's Regulatory Information Management (RIM) environment(s) · Collaborates with data owners to ensure that data is entered into the company's RIM system(s) i ...

Amgen is searching for a Senior Associate to join the R egulatory O ptimization o f T echnical, S urveillance, and S trategic Support (ROOTS2) group within RA CMC. · ...

This role involves performing regulatory activities related to finished products, labelling, · & regulatory database management to ensure compliance with applicable food and other product-related laws · & regulations in accordance with internal processes. · ...

As an associate of Scientific & Regulatory Affairs in the Mars Snacking team you will be performing regulatory activities related to finished products labelling and database management. · ...

Parexel seeks an experienced Regulatory Affairs Professional to join their dynamic team as a Senior Regulatory Affairs Consultant. · ...

This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. The role involves strategic input into development programs, preparation and submission of regulatory documentation, and post-approval lifecycle mana ...

We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. · ...

Parexel is seeking an experienced Regulatory Affairs Professional to join our dynamic team as a Senior Regulatory Affairs Consultant. · ...

We are currently recruiting for a Regulatory Affairs Manager (CTA) with EU experience for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - 1 day per month in the office. · Plan and manage regulatory submissions ( ...

We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist.Create, update and maintain EU Product Information in line with CCDS, Agency RTQ, and current labelling requirements · Serve as the key point ...

At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. · ...