Cmc Regulatory Affairs Associate

**HOW MIGHT YOU DEFY IMAGINATION?** 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. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering...

**PE Global is currently recruiting for a Regulatory Affairs Manager for a leading multi-national Biotech client based in Uxbridge with a hybrid work option.** **Role**: - Responsible for the generation of country specific regulatory strategies and providing feedback to internal teams regarding submission plans and execution of the strategy for one or more...

Regulatory Affairs Consultant - CMC biologics (home or office based)Parexel Uxbridge, England, United KingdomJoin or sign in to find your next jobJoin to apply for the Regulatory Affairs Consultant - CMC biologics (home or office based) role at ParexelContinue with Google Continue with GoogleRegulatory Affairs Consultant - CMC biologics (home or office...

When our values align, there's no limit to what we can achieve.Are you passionate about regulatory affairs in the life science industry? Do you thrive in a dynamic team environment and enjoy managing complex projects? Parexel is seeking a talented Senior Regulatory Affairs Associate with biologics or vaccines background to join our growing team!As a Senior...

Proclinical are recruiting for a Regulatory Affairs Associate to join a pharmaceutical organisation. This role is on a contract basis and is either located in Uxbridge or Cambridge. **Key Skills and Requirements**: - Familiarity in an administrative field within a corporate or similar setting preferably within a healthcare sector. - Educated to a degree...

About The RoleWe are seeking an experienced Regulatory Affairs professional to lead our medical devices and combination products clinical trial regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and serve as the key regulatory representative for our global project teams.The role can...

A leading life sciences consulting firm is seeking a Senior Regulatory Affairs Associate to manage and coordinate regulatory submissions across various markets. Candidates should possess a university degree in life sciences, initial regulatory experience, and proficiency in Module 1 and 3 writing related to biologics or vaccines. The role can be home or...

PE Global 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.You will be working with colleagues who are responsible for leading the European regulatory strategies and...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that...

Role OverviewAn innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and experience to join their team on a 12‑month temporary contract. The role works closely with the regulatory team and core stakeholders across multiple areas, providing regulatory strategy and guidance to ensure deadlines and...