At a Glance
- Tasks: Lead regulatory engagement and develop policy strategies to make a real impact in healthcare.
- Company: Join Kyowa Kirin, a caring and innovative pharmaceutical company dedicated to making people smile.
- Benefits: Enjoy a supportive culture, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with opportunities to represent the company at key industry events.
- Why this job: Be at the forefront of regulatory policy and help shape the future of medicine.
- Qualifications: Experience in pharmaceuticals and regulatory policy, with strong advocacy skills.
The predicted salary is between 80000 - 100000 € per year.
WE PUSH THE BOUNDARIES OF MEDICINE. LEAPING FORWARD TO MAKE PEOPLE SMILE. At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand what really matters to our patients, their families, and their healthcare professionals, helping our people to take bold actions that deliver life-changing solutions sooner. Our culture is rooted in our values: Teamwork, Commitment to Life, Innovation, and Integrity. They help us to push boundaries to deliver extraordinary impact and make KKI a brilliant place to work.
Job Purpose: An experienced regulatory professional, responsible for leading external engagement in the Regulatory and Science Policy forums accessible in the respective region. This entails execution of the Global Regulatory Intelligence Organization (GRIO) process while leading process for the development and submission of Kyowa Kirin’s input externally on regulatory and science policy topics. This position entails Regulatory Policy responsibilities primarily for EU, UK, Switzerland, with limited responsibility for additional markets, e.g. APAC.
Responsibilities:
- Lead/manage the external engagement in the Regulatory and Science Policy forums accessible in the respective regions.
- Represent Kyowa Kirin at relevant external regulatory and science policy conference, industry association working group meetings and forums.
- Represent GRA Regulatory Policy and Intelligence Subfunction and lead Regulatory and Science focused Policy positions in internal forums where government agency and legislative topics are discussed cross-functionally.
- Lead/manage and/or conduct the process for the development and submission of Kyowa Kirin’s input externally on regulatory and science policy topics.
- Develop and/or lead execution of the global/regional regulatory and science policy strateg(ies).
- Lead/manage and/or conduct internal education sessions (e.g. Info Series, Town Hall, Meeting presentations, etc.) on regulatory intelligence topics as needed and/or appropriate.
Qualifications:
- Must have experience working in the pharmaceutical/biotechnology Industry.
- Understanding of Kyowa Kirin’s technologies, products and pipeline preferred.
- Must have experience working in regulatory and science policy role and experience working within industry association groups.
- Proven track record of representation of organization externally and advocate effectively on organization behalf and priorities.
- Prior work experience at a health authority or industry association is a plus.
Associate Director, GRA Policy EMEA/RoW Lead employer: Kyowa Kirin International
At Kyowa Kirin International, we are dedicated to pushing the boundaries of medicine while fostering a culture of teamwork, innovation, and integrity. Our inclusive work environment prioritises employee growth and development, offering opportunities to engage in meaningful projects that directly impact patient care. Located in a vibrant region, we provide our employees with the chance to collaborate with industry leaders and contribute to life-changing solutions, making KKI an exceptional place to build a rewarding career.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, GRA Policy EMEA/RoW Lead
✨Tip Number 1
Network like a pro! Get out there and connect with people in the industry. Attend conferences, webinars, or local meetups related to regulatory affairs. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Show off your expertise! When you get the chance to chat with potential employers or industry peers, don’t hold back on sharing your knowledge about regulatory policies and trends. This will not only showcase your skills but also demonstrate your passion for the field.
✨Tip Number 3
Follow up after meetings or networking events. A quick email thanking someone for their time and mentioning something specific from your conversation can keep you fresh in their mind. Plus, it shows you’re genuinely interested in building relationships.
✨Tip Number 4
Apply through our website! We’ve got some fantastic opportunities at StudySmarter that align with your skills. Don’t just wait for the perfect job to come to you; take the initiative and submit your application directly. It’s a great way to stand out!
We think you need these skills to ace Associate Director, GRA Policy EMEA/RoW Lead
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Associate Director role. Highlight your experience in regulatory and science policy, and show how it aligns with our values at Kyowa Kirin. We want to see how you can push boundaries and make a difference!
Showcase Your Experience:Don’t just list your previous jobs; tell us about your achievements in the pharmaceutical or biotechnology industry. We’re looking for specific examples of how you've led external engagements or represented organisations effectively. Make it personal and impactful!
Be Authentic:Let your personality shine through in your application. We value integrity and commitment to life, so share your passion for making a difference in healthcare. We want to know what drives you and how you can contribute to our mission of making people smile.
Apply Through Our Website:We encourage you to submit your application directly through our website. It’s the best way to ensure it gets into the right hands. Plus, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Kyowa Kirin International
✨Know Your Stuff
Make sure you have a solid understanding of Kyowa Kirin’s technologies, products, and pipeline. Brush up on recent developments in regulatory and science policy, especially those relevant to the EU, UK, and Switzerland. This will show that you're not just interested in the role but are genuinely invested in the company’s mission.
✨Showcase Your Experience
Prepare to discuss your previous experience in the pharmaceutical or biotechnology industry, particularly in regulatory roles. Be ready to share specific examples of how you've successfully represented an organisation in external forums or industry associations. This will demonstrate your capability to lead and manage external engagements effectively.
✨Emphasise Teamwork and Integrity
Kyowa Kirin values teamwork and integrity, so be sure to highlight instances where you've worked collaboratively with others or made ethical decisions in challenging situations. This will resonate well with their culture and show that you align with their core values.
✨Prepare Questions
Have a few thoughtful questions ready to ask at the end of your interview. This could be about their approach to regulatory challenges or how they foster innovation within the team. It shows that you're engaged and thinking critically about how you can contribute to their goals.
