At a Glance
- Tasks: Shape and drive strategic regulatory initiatives to improve patient outcomes.
- Company: Join Roche, a global leader in healthcare innovation.
- Benefits: Flexible working, diverse culture, and opportunities for personal growth.
- Why this job: Make a real impact on healthcare and patient lives.
- Qualifications: Scientific degree and extensive UK regulatory experience required.
- Other info: Collaborative environment with a focus on innovation and diversity.
The predicted salary is between 36000 - 60000 £ per year.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.
Imagine working for an organization that puts people at the heart of everything they do, where your contributions directly impact patient outcomes. At Roche, our number one priority is our patients, and we believe that every person plays a key role in achieving this mission. As a Regulatory Partner at Roche UK, you will be a vital part of our UK Regulatory Chapter. You will leverage your regulatory and scientific expertise to shape and drive strategic initiatives. This is your opportunity to make a difference and be part of a company dedicated to improving lives.
UK Regulatory Group Responsibilities
- The Regulatory group collaborates with the wider business to translate the constantly evolving requirements of the UK regulatory environment into Roche policies, procedures, solutions, and strategies that ensure compliance and maximize the value for patients.
- Our activities encompass:
- Clinical Trial Applications
- National Licensing Applications
- Early Access to Medicines Applications
- National components of medicines authorization via the European Centralized procedure
Who You Are
You are a passionate regulatory expert with a clear vision for improving patient outcomes. With broad and comprehensive expertise within the UK regulatory environment, you will lead foundational work and partner with the business to solve complex regulatory issues impacting the chapter and/or wider business. You will contribute to the development of squad/chapter-based strategic plans and goals, and actively participate in the learning and development of other chapter members. You will have the ability to understand scientific and technical information relating to an assigned portfolio of Roche products.
You also bring:
- A Scientific University degree
- Extensive experience in UK Regulatory Affairs
- Proven experience managing UK submissions post-Brexit
- Experience providing strategic and technical advice
- In-depth knowledge and experience of UK and EU regulatory requirements and procedures
- A proven track record of developing, implementing, and communicating regulatory strategies
- Excellent documentation skills to ensure high-quality and timely submissions
- Experience as a Subject Matter Expert (SME) in defined subject areas or therapeutic areas
- Experience in mentoring peers, as well as managing stakeholder relationships
Who we are
A healthier future drives us to innovate. Together, more than 100,000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. We are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.
LTO -Regulatory Partner in Welwyn employer: F. Hoffmann-La Roche Gruppe
Contact Detail:
F. Hoffmann-La Roche Gruppe Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land LTO -Regulatory Partner in Welwyn
✨Tip Number 1
Network like a pro! Reach out to current or former Roche employees on LinkedIn. Ask them about their experiences and any tips they might have for landing a role as a Regulatory Partner. Personal connections can give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for the interview by diving deep into Roche's mission and values. Understand how your regulatory expertise aligns with their goal of improving patient outcomes. This will help you articulate how you can contribute to their vision during the interview.
✨Tip Number 3
Showcase your adaptability! Be ready to discuss specific examples where you've navigated complex regulatory challenges. Highlighting your problem-solving skills will demonstrate that you're the entrepreneurial spirit they’re looking for.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in being part of Roche’s mission to create a healthier future.
We think you need these skills to ace LTO -Regulatory Partner in Welwyn
Some tips for your application 🫡
Be Yourself: At StudySmarter, we want to see the real you! Don’t be afraid to let your personality shine through in your application. Share your unique qualities and experiences that make you a great fit for the Regulatory Partner role.
Tailor Your Application: Make sure to customise your application to highlight your regulatory expertise and how it aligns with Roche's mission. We love seeing candidates who can connect their skills to our goals of improving patient outcomes.
Showcase Your Experience: We’re looking for someone with a solid background in UK Regulatory Affairs. Be sure to detail your relevant experience, especially post-Brexit submissions and strategic advice. This will help us understand how you can contribute to our team.
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 ensure you’re considered for the role. Plus, it makes the process smoother for everyone involved.
How to prepare for a job interview at F. Hoffmann-La Roche Gruppe
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of UK regulatory affairs, especially post-Brexit changes. Be ready to discuss how these regulations impact patient outcomes and how you can contribute to Roche's mission.
✨Show Your Passion for Patients
Roche values individuals who are passionate about improving patient outcomes. Prepare examples from your past experiences where your work directly impacted patients or contributed to better healthcare solutions.
✨Demonstrate Collaboration Skills
Since the role requires effective cross-functional collaboration, think of instances where you've successfully worked with diverse teams. Highlight your ability to negotiate and influence stakeholders, as this will be crucial in your role as a Regulatory Partner.
✨Be Yourself
Roche encourages personal expression, so don’t hesitate to show your unique qualities during the interview. Authenticity can set you apart, so share your story and how it aligns with Roche’s values and mission.