This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Join Amgen in Uxbridge, UK as a Sr Associate Regulatory Affairs - CMC. Leverage your CMC background in Quality or Manufacturing to drive global regulatory submissions. This role offers vast growth opportunities, a diverse community, and a generous Total Rewards Plan. Ideal for proactive professio...
Location
United Kingdom , Uxbridge
Salary
Not provided
Amgen
Expiration Date
Until further notice
Vice President, Regulatory Affairs
Lead regional regulatory strategy for Amgen in Uxbridge, UK, driving innovation in Oncology, Inflammation, and Rare Disease. This VP role requires 8+ years of industry experience, deep regulatory expertise, and proven leadership in a global matrix organization. You will shape external environment...
Location
United Kingdom , Uxbridge
Salary
Not provided
Amgen
Expiration Date
Until further notice
Eu Regulatory Affairs Senior Manager (Biosimilars)
Amgen seeks a Senior Manager in EU Regulatory Affairs for Biosimilars in Uxbridge, UK. You will lead regional regulatory strategy and submissions for a dynamic biosimilar portfolio. Ideal candidates possess deep biosimilars expertise, a scientific degree, and a proven track record in regulatory s...
Location
United Kingdom , Uxbridge
Salary
Not provided
Amgen
Expiration Date
Until further notice
Eu Regulatory Affairs Senior Manager - General Medicine
Senior EU Regulatory Affairs Manager sought to lead regional strategy and submissions for General Medicine at Amgen in Cambridge/Lisbon. Drive clinical trial and marketing applications, leveraging deep drug lifecycle knowledge and regulatory expertise. Requires a scientific degree, proven strateg...
Location
United Kingdom; Portugal , Cambridge; Lisbon
Salary
Not provided
Amgen
Expiration Date
Until further notice
Senior Associate Regulatory Affairs
Senior Associate Regulatory Affairs role in Cambridge, UK, supporting UK and Ireland submissions. You will manage marketing authorisations, clinical trial documentation (IMPDs), and agency interactions with increasing autonomy. Requires degree, Veeva Vault experience, and strong regulatory projec...
Location
United Kingdom , Cambridge
Salary
Not provided
Amgen
Expiration Date
Until further notice
We use cookies to enhance your experience, analyze traffic, and serve personalized content. By clicking “Accept”, you agree to the use of cookies.