EU Regulatory Affairs Manager

Amgen Inc. (IR); Uxbridge; Hybrid; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Hybrid work flexibility

Total rewards package

Job summary

Amgen Inc. in the United Kingdom (Uxbridge/Cambridge hybrid) seeks an EU Regulatory Affairs Manager to lead submissions for clinical trials and marketed products.

You will craft regional regulatory strategies, provide guidance for regulatory documents, and ensure compliance with EU requirements across the product lifecycle. The role requires experience with regulatory procedures (scientific advice, orphan apps, PIP, MA) and strong communication.

Qualifications

• Degree-educated with experience in regulatory roles.
• Experience registering products and leading EU filings.
• Knowledge of EU legislation and regulatory policy.

Responsibilities

• Plan and manage regulatory submissions for clinical trials and marketing applications.
• Develop and execute regional regulatory product strategies.
• Provide regulatory guidance for regional documents and meetings.
• Monitor regulatory developments and assess impact on products.

Skills

Regulatory strategy

Regulatory submissions

EU regulatory knowledge

Communication skills

Education

Bachelor's degree in life sciences or related field

Advanced degree preferred

Tools

AI tools basic

Job description

**EU REGULATORY AFFAIRS MANAGER****LIVE****What you will do**In this vital role you will work to ensure that Amgen acquires and maintains all the required EU licenses in order to support clinical trials for investigational medicinal products as well as marketed medicinal products.You will support one or more products from an EU regulatory perspective.Strategy and Execution* Depending on business needs and experience, the role may include EU Regulatory Lead responsibility for one or more products.* Plan and manage regulatory submissions (e.g. clinical trial and marketing applications) for products within Amgen's portfolio in compliance with global filing plans and EU regional regulatory requirements.* Under general supervision, implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with EU regional legislation and regulatory requirements. Provide content guidance for regional regulatory documents and meetings in accordance with global strategy.* Provide regulatory guidance on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, scientific advice, Orphan Drug, MA approval mechanisms and paediatric plans).* Support EU label negotiation activities.* Under general supervision participate in the development and execution of regional regulatory product strategies.* Under general supervision, develop predictions for expectations and risks associated with outcomes by regulatory agencies.Regulatory Research* Maintain an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to Amgen products.* Perform regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement.* Under supervision evaluate and communicate impact of relevant regional regulations, guidances, current regulatory environment and competitor labelling.**Be part of our team**We are currently looking for x3 EU Regulatory Affairs Managers between Portugal and the United Kingdom, joining the EU Oncology or General Medicine teams, part of the Global Regulatory Affairs function in Europe.You will be working with colleagues who are responsible for leading the European regulatory strategies and submissions for development and marketed products from first-in human clinical trials to marketing authorisation, and throughout the products lifecycle.**WIN****What we expect of you** We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:* Degree educated and previous experience in a similar role* Hands-on experience with registration procedures in the region, such as clinical trials, pre-MAA regulatory procedures (eg scientific advice, orphan applications or Paediatric Investigation Plans (PIPs)), MA, post-approval changes, extensions and renewals* Experience developing regulatory strategies for products in clinical development and post-marketing phases.* Knowledge of EU legislation and regulations relating to medicinal products* Working with policies, procedures and SOP’s .* Strong communication skills - both oral and written.* Ability to anticipate and prevent potential issues.* Ability to resolve conflicts and develop a course of action leading to a beneficial outcome.* Basic proficiency in using AI tools to support day-to-day work.**THRIVE****What you can expect of us** As we work to develop treatments that take care of others, we work to care for our teammates’ professional and personal growth and well-being. * Growth opportunities to learn and move up and across our global organization* Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act* Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits**LOCATION:**Flexibility to work from home with few days per month working from our Cambridge or Uxbridge offices. **APPLY NOW****for a career that defies imagination**In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.**careers.amgen.com**Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.