At a Glance
- Tasks: Lead regulatory strategies for innovative drugs and ensure compliance with global standards.
- Company: Viatris, a global healthcare leader committed to empowering healthier lives.
- Benefits: Career progression, work-life balance, health insurance, and a bonus scheme.
- Other info: Join a diverse and inclusive team dedicated to corporate social responsibility.
- Why this job: Make a real impact in global healthcare while shaping the future of drug regulations.
- Qualifications: Advanced degree and extensive regulatory leadership experience required.
The predicted salary is between 80000 - 100000 £ per year.
Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, Viatris provides access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases. Viatris is committed to education, outreach and better access to treatment and fosters a collaborative culture that encourages courage and resilience.
The Head of Regulatory Affairs Strategy is a senior level position responsible for developing regulatory strategies to advance Viatris' global portfolio of innovative, brand and marketed drugs. This role provides strategic direction across development and post-approval life-cycle, engages with global health authorities to define regulatory strategies that enable product approvals aligned with company plans, and communicates a strategic vision while ensuring regulatory compliance and priority setting.
Key responsibilities and expectations:
- Provides leadership, strategic direction, and managerial oversight to the Viatris Global Regulatory Strategy team to ensure timely and successful submissions of drug applications to global regulatory agencies that enable timely approval.
- Establishes and maintains strong partnerships with Global, Regional, and Local stakeholders from cross-functional disciplines to foster development and implementation of strategies that expedite registration of new products, line extensions, and post-approval and lifecycle maintenance changes through risk identification and mitigation.
- Provides input into new business development opportunities.
- Ensures coordination and implementation of consistent standards and processes across Global Strategic regulatory teams, aligning with regulatory processes, global policies, regulations, and leadership priorities.
- Sets team objectives and operational/strategic plans aligned to the Global Regulatory Affairs direction and other key stakeholders (R&D, Drug Safety, Clinical, Operations, Commercial and Medical).
- Supports development and maintenance of excellent relationships with global regulatory agencies to influence future regulations and resolve project/compound/product issues.
- Supports Regulatory Affairs partners in developing and maintaining local regulatory agency relationships.
- Partners with corporate affairs, government affairs, and other local policy leaders to achieve business policy objectives.
- Defines roles and competencies of the Global Strategy team and implements strategies to enhance capacity and capabilities.
- Collaborates with regulatory colleagues across functions to harmonize practices and deliver a unified Viatris voice.
- Drives continuous improvement in regulatory processes, systems, and capabilities.
- Directs opportunities including training, rotational development, and succession planning for the global strategy team.
Qualifications:
- A higher degree (MS, PhD, PharmD, MBA) is preferred.
- Extensive global regulatory leadership experience, with experience in a relevant technical field (e.g., R&D, Clinical, Quality, Technical Services).
- Demonstrable strategic experience across the drug development and commercial lifecycle, with proven contributions.
- Experience with innovative, branded products and generic drug regulatory submissions and approvals, DMFs, CEP filings, and development of global compendial requirements.
- Experience with diverse dosage forms, including sterile products and drug-device combination products is desirable.
- Global regulatory experience including knowledge of clinical trials strategy, new product submission processes and lifecycle management.
- Line management and senior leadership experience.
- Proven ability to deliver effectively in a complex matrix environment.
- Knowledge of global policies, regulations, and guidelines with extensive technical and industry knowledge to shape project strategies and reduce regulatory burden across markets.
- Understanding of current and emerging regulatory requirements and ability to lead negotiations with regulatory authorities for projects and policy initiatives.
- Ability to collaborate with Regulatory, Manufacturing & Supply Chain, Quality, Safety, Medical, Commercial, Legal and senior stakeholders to achieve objectives.
Benefits:
- Excellent career progression opportunities
- Work-life balance initiatives
- Bonus scheme
- Health insurance
- Pension
Diversity, Inclusion & Sustainability: Viatris values diversity and inclusion as essential to its mission and fosters diversity, equity and inclusion across the business. Corporate social responsibility is foundational to Viatris, with ongoing efforts in responsible and sustainable operations.
Head of Regulatory Affairs Strategy in Hatfield employer: Viatris
Viatris is an exceptional employer that prioritises employee growth and well-being, offering excellent career progression opportunities and a strong commitment to work-life balance. With a collaborative culture that values diversity, inclusion, and sustainability, employees are empowered to make meaningful contributions while enjoying comprehensive benefits such as health insurance and a bonus scheme. Located in a dynamic healthcare environment, Viatris provides a unique opportunity to influence global regulatory strategies and improve access to high-quality medicines for patients worldwide.
StudySmarter Expert Advice🤫
We think this is how you could land Head of Regulatory Affairs Strategy in Hatfield
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those already at Viatris. A friendly chat can open doors and give you insights that might just set you apart from the crowd.
✨Tip Number 2
Prepare for interviews by diving deep into Viatris' mission and values. Show us how your experience aligns with our goals in regulatory affairs. We love candidates who are genuinely passionate about making a difference!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop us a quick thank-you note. It shows your enthusiasm and keeps you fresh in our minds as we make decisions.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at Viatris.
We think you need these skills to ace Head of Regulatory Affairs Strategy in Hatfield
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Head of Regulatory Affairs Strategy role. Highlight your relevant experience in regulatory leadership and strategic development, as this will show us that you understand what we're looking for.
Showcase Your Achievements:When detailing your past roles, focus on specific achievements that demonstrate your ability to lead and influence regulatory strategies. We love seeing quantifiable results, so don’t hold back on the numbers!
Be Clear and Concise:Keep your application clear and to the point. Use straightforward language and avoid jargon unless it’s necessary. We appreciate clarity, especially when it comes to complex regulatory topics.
Apply Through Our Website:We encourage you to apply directly through our website. This ensures your application gets to the right people quickly and helps us keep track of all candidates efficiently. Plus, it’s super easy!
How to prepare for a job interview at Viatris
✨Know Your Regulatory Landscape
Before the interview, brush up on the latest global regulatory policies and guidelines relevant to Viatris. Understanding the nuances of drug development and approval processes will show your expertise and readiness for the Head of Regulatory Affairs Strategy role.
✨Showcase Your Leadership Skills
Prepare examples that highlight your leadership experience in a complex matrix environment. Discuss how you've successfully led teams, managed cross-functional collaborations, and driven strategic initiatives in regulatory affairs.
✨Align with Company Values
Familiarise yourself with Viatris' mission and values, especially their commitment to diversity, inclusion, and corporate social responsibility. Be ready to discuss how your personal values align with theirs and how you can contribute to fostering a collaborative culture.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and strategic thinking. Think about past challenges you've faced in regulatory affairs and how you navigated them, particularly in relation to innovative and branded products.