Regulatory Affairs Manager – Medical Devices, Cosmetics and Food Supplements

tendersglobal
Huddersfield
13 hours ago
Create job alert
Job title:

Regulatory Affairs Manager – Medical Devices, Cosmetics and Food Supplements


Company

STADA Arzneimittel


Job description

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 | PermanentRole PurposeAs 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.

Desirable Attributes



  • 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 youAt 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.💉 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.⚡ Electric Car Scheme through Octopus Energy, plus free on-site EV charging.🚲 Cycle to Work Scheme.👪 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.


Expected salary
Location

Huddersfield


Job date

Wed, 20 Aug 2025 01:30:25 GMT



#J-18808-Ljbffr

Related Jobs

View all jobs

Regulatory Lead - Medical Devices, Cosmetics & Supplements

Regulatory Affairs Manager

Global Quality Manager

Regulatory Affairs Manager

Regulatory Affairs Manager

Senior Regulatory Affairs Manager, Medical Devices

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Neurodiversity in Medical Technology Careers: Turning Different Thinking into a Superpower

Medical technology sits at the intersection of health, engineering & innovation. From imaging & diagnostics to digital health apps, wearables & surgical robotics, medtech is about solving complex real-world problems that directly affect patients’ lives. To do that well, the sector needs people who think differently. If you live with ADHD, autism or dyslexia, you may have been told your brain is “too distracted”, “too literal” or “too disorganised” for a regulated, safety-critical industry. In reality, many traits that made school or previous jobs difficult can be huge strengths in medical technology – from pattern-spotting in clinical data to meticulous attention to detail in device testing. This guide is for neurodivergent job seekers exploring medical technology careers in the UK. We’ll cover: What neurodiversity means in a medtech context How ADHD, autism & dyslexia strengths map to common medtech roles Practical workplace adjustments you can ask for under UK law How to talk about your neurodivergence in applications & interviews By the end, you’ll have a clearer sense of where you might thrive in medical technology – & how to turn “different thinking” into a genuine superpower.

Medical Technology Hiring Trends 2026: What to Watch Out For (For Job Seekers & Recruiters)

As we move into 2026, the medical technology (MedTech) jobs market in the UK is changing fast. Hospitals and health systems are under pressure to do more with less. Diagnostics and devices are becoming smarter, more connected and more regulated. AI, robotics and remote monitoring are no longer “future tech” – they’re being built into mainstream care pathways. At the same time, budgets are tight, funding cycles are uneven and some healthtech start-ups are consolidating or being acquired. That means fewer vague “innovation” roles and more focus on medical technology jobs that directly support regulatory approval, patient safety, NHS adoption and commercial growth. Whether you are a MedTech job seeker planning your next move, or a recruiter building teams for medical device, diagnostics or digital health companies, this guide breaks down the key medical technology hiring trends for 2026.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.