Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Ensure safety compliance and manage critical pharmacovigilance activities.
- Company: Join Amgen, a leading biotechnology company dedicated to serving patients worldwide.
- Benefits: Flexible work options, generous rewards, and opportunities for personal growth.
- Why this job: Make a real impact in patient safety while collaborating with global teams.
- Qualifications: Life science degree and experience in pharmacovigilance required.
- Other info: Be part of a diverse team that values your unique contributions.
The predicted salary is between 36000 - 60000 ÂŁ per year.
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 ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
What you will do
- In this vital role you will be responsible for ensuring adherence to Amgen’s regulatory commitment for pharmacovigilance.
- You will provide management of a subset of safety activities within the UK and Ireland affiliate, working with both local and global colleagues, and based on sound knowledge of pharmacovigilance regulations and company procedures.
Pharmacovigilance Legislation: Maintain own current knowledge of and compliance with local safety regulations.
Case management: Perform business critical “core” safety activities per legal deadlines including intake of AE reports, follow up with HCPs for complete data, ICSR report submission to regulators. Handling safety enquiries received to the departmental inbox from both internal and external stakeholders. Review metrics to monitor MHRA & HPRA submission compliance and share with Qualified Person for Pharmacovigilance (QPPV)/Regional Management.
Periodic Reporting: Assist with submission of DSUR and PSUR safety reports to Regulators and Ethics Committees where applicable. Perform review of relevant PSUR safety signals for MHRA notification.
Risk Management: Support for safety risk communications (e.g. Dear Investigator Letter, Urgent Safety Measures, Risk Minimisation Materials etc.) and Risk Management Plans in conjunction with Regulatory Affairs, Clinical and Medical Departments. Maintain awareness of safety profiles of designated Amgen products and new risk information.
Leadership: Provide management of a subset of safety activities, whilst reporting to the Senior Global Safety Manager. Provide input into cross functional programs, to reflect local requirements or operating environment. Support with process improvement initiatives and implementation of legislative changes. Serve as a safety subject matter expert with the affiliate.
Deputise: Assist Senior Global Safety Manager / Country Safety Lead with escalation of issues to Regional Management / QPPV, and support with issue resolution. Deputise for Senior Global Safety Manager when necessary.
Be part of our team
You will be joining the UK & Ireland Safety Team, based in the local affiliate, and collaborating with other affiliate functions and also with Global Patient Safety colleagues to meet business needs. Together with team members, you will conduct business critical safety tasks, provide support to audits and inspections, and assist the Senior Global Safety Manager with activities and issue resolution where necessary. Within the team, you will maintain awareness of current prescribing information, safety profile and new risk information for designated Amgen products, to support product safety activities.
What we expect of you
- Graduate with life science or healthcare degree and proven relevant industry experience within post market and clinical trial pharmacovigilance.
- Use of MS Office products to a proficient standard – Word, Excel, PowerPoint.
- Deep knowledge of processes and regulations in pharmacovigilance.
- Experience with Safety Databases.
- Strong initiative and problem‑solving skills.
- Natural team player with the personal qualities to relate well to people at all levels.
- Aptitude for analytical thinking, with a methodical approach and unquestionable attention to detail.
- Highly motivated, quick to learn, with ability to work effectively under own initiative and a strong drive for excellence.
What you can expect of us
- Vast 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: Ability to work flexibly from home with occasional office work from our Cambridge next generation workspace.
APPLY NOW for a career that defies imagination.
Global Safety Manager in Cambridge employer: Amgen SA
Contact Detail:
Amgen SA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Safety Manager in Cambridge
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Amgen on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Brush up on pharmacovigilance regulations and be ready to discuss how your experience aligns with Amgen's mission. Show them you're not just a fit for the role, but for the company culture too.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources to get comfortable with common questions. The more you practice, the more confident you'll feel when it’s time to shine.
✨Tip Number 4
Don’t forget to follow up! After your interview, send a thank-you email to express your appreciation for the opportunity. It shows your enthusiasm and keeps you fresh in their minds as they make their decision.
We think you need these skills to ace Global Safety Manager in Cambridge
Some tips for your application 🫡
Show Your Passion: When writing your application, let your enthusiasm for the role shine through! We want to see how your passion for pharmacovigilance and patient safety aligns with our mission at Amgen.
Tailor Your CV: Make sure to customise your CV to highlight relevant experience in pharmacovigilance. We love seeing how your background fits with the specific responsibilities of the Global Safety Manager role.
Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so make sure your skills and experiences are easy to spot and understand!
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role.
How to prepare for a job interview at Amgen SA
✨Know Your Pharmacovigilance Stuff
Make sure you brush up on your knowledge of pharmacovigilance regulations and case management processes. Be ready to discuss how you've handled safety activities in the past, as this will show your understanding of the role and its responsibilities.
✨Show Your Team Spirit
As a Global Safety Manager, collaboration is key. Prepare examples of how you've worked effectively within a team, especially in cross-functional settings. Highlight your ability to relate well to people at all levels, as this will resonate with their emphasis on teamwork.
✨Be Ready for Problem-Solving Questions
Expect questions that assess your initiative and problem-solving skills. Think of specific instances where you've tackled challenges in pharmacovigilance or safety reporting, and be prepared to explain your thought process and the outcomes.
✨Demonstrate Your Attention to Detail
Given the nature of the role, attention to detail is crucial. Prepare to discuss how you ensure compliance with safety regulations and how you monitor metrics for submission compliance. This will show that you take the responsibilities seriously and are committed to excellence.