At a Glance
- Tasks: Lead medical strategy and governance for STADA UK's Consumer Healthcare portfolio.
- Company: Join a growing team at STADA UK, committed to caring for people's health.
- Benefits: Enjoy competitive salary, hybrid working, and extensive employee benefits.
- Other info: Collaborative culture with opportunities for personal and professional growth.
- Why this job: Make a real impact in healthcare by driving innovation and scientific excellence.
- Qualifications: Degree in Medicine, Pharmacy, or Life Sciences with significant Medical Affairs experience.
The predicted salary is between 63000 - 77000 £ per year.
- Associate Director Medical Affairs | Consumer Healthcare
- Reading (Hybrid)
STADA UK Thornton & Ross is on an exciting growth journey with more than 700 employees being fully committed to our purpose of Caring for People’s Health as a Trusted Partner.
Together we are shaping the future of Thornton & Ross by living our values of Integrity, Entrepreneurship, Agility and One STADA.
If you want to work in an open culture where your uniqueness is valued, join our Team.
About The Role
As the Associate Director Medical Affairs, you will lead the medical strategy, governance and scientific activities for STADA UK's Consumer Healthcare portfolio.
Acting as the senior medical lead, you’ll ensure commercial decisions, product claims and innovation initiatives are grounded in robust scientific evidence and aligned with regulatory and compliance requirements.
Additionally, you’ll provide leadership across the broader Medical Affairs team, driving excellence and collaboration across both Consumer Healthcare and Specialty portfolios.
- How You Will Make An Impact
- Consumer Healthcare Medical Strategy
- Act as the medical lead for the Consumer Healthcare portfolio.
- Provide scientific leadership to support portfolio growth, innovation, and lifecycle management.
- Ensure medical perspectives are embedded in commercial and portfolio decision-making.
- Translate developments in self-care, pharmacy practice and relevant therapeutic areas into actionable business recommendations.
- Scientific and Claims Governance
- Ensure all product claims are supported by robust scientific evidence.
- Provide medical review and approval of promotional and non-promotional materials.
- Develop claims substantiation strategies for new and existing products.
- Ensure compliance with PAGB, CAP Code, and internal procedures, acting as a trusted scientific advisor to internal teams.
- Portfolio Development & Innovation
- Offer medical insights into product development, reformulation, and lifecycle management activities.
- Assess new product opportunities and portfolio expansion initiatives.
- Evaluate emerging scientific evidence and consumer trends to identify opportunities and risks.
- Support launch readiness activities for new products and line extensions.
- Leadership & Team Development
- Lead and develop a team of Medical Affairs professionals (3-4 direct reports).
- Foster a high-performing, collaborative and accountable team culture.
- Drive the development of scientific capability and ensure clear objectives across the team.
- Cross-Functional Collaboration
- Partner with Regulatory Affairs, Quality, Pharmacovigilance, Commercial and Portfolio teams.
- Provide medical support for regulatory submissions, safety assessments and product quality issues.
- Contribute to the development of effective customer-facing communications.
- Operational Excellence
- Continuously improve Medical Affairs processes and ways of working.
- Ensure efficient use of resources and maintain high-quality delivery of medical activities.
- Drive accountability, simplicity, and execution excellence across the function.
- What Makes You a Great Fit
- Education: Degree in Medicine, Pharmacy, or Life Sciences.
• Experience
- Significant experience in pharmaceutical or consumer healthcare Medical Affairs.
- Proven leadership in medical strategy and scientific activities, with experience managing and developing teams.
- Strong knowledge of UK regulatory frameworks, ABPI Code and PAGB Code.
- Desirable: Medical signatory experience, OTC or Consumer Healthcare background and exposure to specialty medicines.
• Skills
- Strong scientific credibility and ability to translate complex science into business insights.
- Exceptional leadership, stakeholder management, and collaboration skills. Commercial awareness with the ability to balance scientific integrity and business objectives.
- Operational excellence in planning, prioritisation and execution.
- How We Care For You
- Competitive salary, car allowance and annual bonus scheme.
- Salary Sacrifice Pension Scheme offering 8% employer contribution rates.
- Hybrid working – we spend three days of your choice in the office, with the remaining days working at home.
- 25 days of annual leave plus bank holidays with the potential to buy up to 5 additional days.
- Private Health cover benefits
- Life Assurance cover
- Free winter flu jab.
- Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family.
- Cycle to Work Scheme.
- Enhanced Family Leave.
- many more employee benefits & celebration events.
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Associate Director Medical Affairs in Reading employer: STADA Thornton & Ross
STADA Thornton & Ross is an exceptional employer located in Reading, offering a dynamic work environment that fosters innovation and collaboration. With a strong focus on employee growth, we provide opportunities for professional development alongside competitive salaries, hybrid working options, and comprehensive health benefits, making it an ideal place for those looking to make a meaningful impact in the healthcare sector.
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We think this is how you could land Associate Director Medical Affairs in Reading
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We think you need these skills to ace Associate Director Medical Affairs in Reading
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at STADA Thornton & Ross that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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