At a Glance
- Tasks: Lead regulatory engagement and represent Kyowa Kirin in policy forums.
- Company: Join a caring and innovative pharmaceutical company dedicated to making a difference.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic role with opportunities to influence industry standards.
- Why this job: Make a real impact in healthcare by shaping regulatory policies.
- Qualifications: Experience in pharmaceuticals and regulatory science policy required.
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.
Key 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.
Position Requirements: 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 in Marlow employer: Kyowa Kirin International
At Kyowa Kirin International, we are dedicated to making a meaningful impact in the pharmaceutical industry while fostering a culture of teamwork, innovation, and integrity. Our inclusive work environment encourages professional growth and development, offering employees the opportunity to engage in life-changing projects that truly matter. Located in a vibrant region, we provide our team with unique advantages such as access to leading regulatory forums and a chance to represent our values on an international stage.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director, GRA Policy EMEA/RoW Lead in Marlow
✨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, don’t hold back on sharing your knowledge about regulatory policies and trends. This will not only demonstrate your passion but also position you as a valuable asset.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way. Use this opportunity to reiterate your interest in the role and mention something specific from the conversation that excited you. It keeps you fresh in their minds!
✨Tip Number 4
Apply through our website! We’ve got some fantastic opportunities waiting for you at StudySmarter. By applying directly, you’ll ensure your application gets the attention it deserves, and you’ll be one step closer to joining a team that’s all about making a difference.
We think you need these skills to ace Associate Director, GRA Policy EMEA/RoW Lead in Marlow
Some tips for your application 🫡
Show Your Passion:When writing your application, let your enthusiasm for the pharmaceutical industry shine through. We want to see how your values align with ours, especially around making a difference and pushing boundaries.
Tailor Your CV:Make sure your CV is tailored to highlight your experience in regulatory and science policy. We’re looking for specific examples that demonstrate your expertise and how you’ve made an impact in previous roles.
Craft a Compelling Cover Letter:Your cover letter is your chance to tell us why you’re the perfect fit for this role. Be sure to connect your past experiences with the responsibilities outlined in the job description, and don’t forget to mention your understanding of our mission.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re proactive and keen to join our team!
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 specific examples from your past roles where you've successfully engaged with regulatory and science policy forums. Highlight any experience you have with industry associations or health authorities, as this will demonstrate your capability to represent the organisation effectively.
✨Emphasise Teamwork and Innovation
Kyowa Kirin values teamwork and innovation, so be ready to discuss how you've collaborated with others to achieve common goals. Share instances where your innovative thinking led to successful outcomes in regulatory processes or policy development.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to regulatory challenges and their future strategies. This not only shows your interest but also gives you a chance to assess if the company culture aligns with your values, particularly around commitment to life and integrity.
