At a Glance
- Tasks: Lead regulatory activities for medical devices, cosmetics, and food supplements while ensuring compliance.
- Company: Join STADA UK Thornton & Ross, a growing company dedicated to caring for people's health.
- Benefits: Enjoy hybrid working, competitive salary, health benefits, and a supportive wellbeing programme.
- Why this job: Be part of a diverse team shaping the future of healthcare with impactful products.
- Qualifications: Degree in Life Sciences or related field; 5+ years in Regulatory Affairs preferred.
- Other info: Open to applicants from non-pharmaceutical backgrounds; we value uniqueness and inclusivity.
The predicted salary is between 36000 - 60000 ÂŁ per year.
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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 Regulatory Team.
STADA UK Thornton & Ross – Regulatory Affairs Manager – Medical Devices, Cosmetics and Food Supplements
Huddersfield |U.K.| Full-time | Permanent
Role Purpose
As Regulatory Affairs Manager – Non Pharma, you will lead and manage regulatory activities for non-pharmaceutical products, including cosmetics, medical devices and food supplements. You will ensure compliance with applicable UK and EU regulations, support product development and lifecycle management, and act as a key liaison with regulatory authorities and internal stakeholders.
Your Impact in This Role
- Lead the development and execution of regulatory strategies across non-pharmaceutical product categories (e.g. medical devices, cosmetics, food supplements), ensuring speed to market and compliance.
- Evaluate product classification, claims, and risk/benefit to guide regulatory planning, submissions, and portfolio lifecycle decisions.
- Prepare, review, and submit regulatory dossiers and notifications (e.g. CPNP for cosmetics), ensuring timely and “fit for purpose” registrations in local and international markets.
- Represent the business in interactions with regulatory authorities, licensing partners, and trade associations (e.g. PAGB, CTPA), proactively communicating outcomes across the organisation.
- Collaborate cross-functionally with Quality, Marketing, Product Development, and Supply Chain to align regulatory input with business goals at all project stages.
- Oversee regulatory review and sign-off of product artwork and promotional materials in compliance with local legislation and Codes of Practice.
- Maintain oversight of documentation, systems (e.g. sDMS), and readiness for internal audits and inspections.
- Lead and develop the regulatory team: manage resource allocation, support succession planning, and ensure all activities align with Health & Safety and Quality standards.
- Co-manage a regulatory budget of over €2 million, ensuring optimal resource use aligned with changing business priorities.
- Provide regulatory input during due diligence processes and integration of new products or acquisitions.
What We\’re Looking For
- A degree in Life Sciences, Pharmacy, Chemistry, or a related discipline.
- At least 5 years of experience in Regulatory Affairs, ideally within non-pharmaceutical categories such as medical devices, cosmetics, or food supplements.
- A solid track record in navigating complex regulatory landscapes and supporting successful product launches and lifecycle management.
- Substantial experience in the consumer goods industry — preferably within consumer healthcare and/or cosmetics.
- In-depth knowledge of UK and EU regulatory frameworks for cosmetics, medical devices, and food supplements (licenced medicines experience would be desirable, but not mandatory) .
- Practical experience with regulatory submissions and direct engagement with health authorities.
- Strong communication, project management, and organisational skills, with the ability to work cross-functionally in a dynamic environment.
- Experience working in a matrixed or global organisation.
- Ability to interpret complex regulations and translate them into practical business-relevant guidance.
- Proactive, detail-oriented, and capable of managing multiple priorities simultaneously.
How we care for you
At Thornton & Ross our purpose “Caring for people’s health as a trusted partner” motivates us every day. And what would be a better place than starting with our own employees. Which is why we give much in return:
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.
Health benefits provided through our Vitality Private Medical Insurance.
Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family.
Electric Car Scheme through Octopus Energy, plus free on-site EV charging.
Enhanced Family Leave.
Plus, many more employee benefits & celebration events.
STADA Group values and promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology, or sexual orientation. We use the strength of our uniqueness to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation, and the promotion of an inclusive working environment. We are looking forward to your application and welcome applications without a pharmaceutical background.
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Regulatory Affairs Manager - Medical Devices, Cosmetics and Food Supplements employer: STADA Arzneimittel AG
Contact Detail:
STADA Arzneimittel AG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager - Medical Devices, Cosmetics and Food Supplements
✨Tip Number 1
Familiarise yourself with the specific UK and EU regulations related to medical devices, cosmetics, and food supplements. Understanding these frameworks will not only help you in interviews but also demonstrate your commitment to compliance and regulatory excellence.
✨Tip Number 2
Network with professionals in the regulatory affairs field, especially those who have experience in non-pharmaceutical categories. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends and challenges in the sector.
✨Tip Number 3
Prepare to discuss your experience with regulatory submissions and interactions with health authorities. Be ready to share specific examples of how you've navigated complex regulatory landscapes and contributed to successful product launches.
✨Tip Number 4
Showcase your project management skills by discussing how you've managed multiple priorities in a dynamic environment. Highlight any cross-functional collaboration experiences that align with the role's requirements, as this will resonate well with the hiring team.
We think you need these skills to ace Regulatory Affairs Manager - Medical Devices, Cosmetics and Food Supplements
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in Regulatory Affairs, particularly within non-pharmaceutical categories like medical devices, cosmetics, and food supplements. Use specific examples to demonstrate your knowledge of UK and EU regulatory frameworks.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for the role and the company. Mention how your values align with STADA's commitment to caring for people's health and how your unique skills can contribute to their regulatory team.
Showcase Your Achievements: In your application, include quantifiable achievements from your previous roles, such as successful product launches or compliance projects. This will help illustrate your capability to navigate complex regulatory landscapes.
Proofread and Edit: Before submitting your application, thoroughly proofread your documents for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in Regulatory Affairs.
How to prepare for a job interview at STADA Arzneimittel AG
✨Know Your Regulations
Familiarise yourself with the UK and EU regulatory frameworks for medical devices, cosmetics, and food supplements. Be prepared to discuss specific regulations and how they impact product development and lifecycle management.
✨Showcase Your Experience
Highlight your previous experience in Regulatory Affairs, especially within non-pharmaceutical categories. Prepare examples of successful product launches and how you navigated complex regulatory landscapes.
✨Demonstrate Cross-Functional Collaboration
Emphasise your ability to work collaboratively with various teams such as Quality, Marketing, and Product Development. Share instances where your regulatory input aligned with business goals and contributed to project success.
✨Prepare for Scenario Questions
Anticipate scenario-based questions that assess your problem-solving skills and ability to manage multiple priorities. Think about how you would handle regulatory challenges or conflicts with stakeholders.