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- Tasks: Lead global regulatory submissions for medicinal products and collaborate across diverse markets.
- Company: Karo Healthcare is a dynamic personal-care retail company with a portfolio of over 80 brands worldwide.
- Benefits: Enjoy a flexible schedule, hybrid work model, and opportunities for personal growth.
- Why this job: Join a fast-growing company where your work directly impacts healthcare and customer satisfaction.
- Qualifications: University degree in Life Sciences and 5+ years in Regulatory Affairs, especially with medicinal products.
- Other info: Karo Healthcare values diversity and inclusivity, welcoming candidates from all backgrounds.
The predicted salary is between 43200 - 72000 £ per year.
Karo Healthcare, a dynamic and growing personal-care retail company, is all about making smart choices for everyday healthcare. With a wide-ranging portfolio across seven categories including medical products, we own and sell over 80 brands in about 90 countries. Our core belief in empowering people to make intelligent health decisions drives our growth strategy, blending organic expansion and M&A. Join us at Karo Healthcare on our exciting journey.
We are currently looking for a Global Regulatory Affairs Manager for our office in Maidenhead, UK.
What’s in it for you?
- A unique chance to join a fast-growing, international company where you’ll own critical submissions across a global portfolio.
- You’ll work independently, yet cross-functionally - engaging with diverse markets, including the Middle East, Africa, and Asia.
- If you’re ready to bring structure, strategy, and energy to a hands-on regulatory role, this is your opportunity to grow.
What you’ll be doing
- Lead and manage regulatory submissions for medicinal products across assigned global regions.
- Coordinate and prepare regulatory documentation (excluding core dossier creation).
- Ensure compliant, up-to-date product artworks and labelling, including serialization requirements.
- Manage artwork updates and ensure local compliance.
- Collaborate cross-functionally to provide strategic regulatory input.
- Support geo expansion, launch in new markets for currently registered products.
- Coordinate with subsidiaries, partners, consultants, and publishing vendors.
- Oversee translations and ensure up to date local product databases and websites.
- Maintain and update internal RIM systems and IDMP/SPOR.
- Contribute to the development and upkeep of internal SOPs.
- Stay up to date with evolving global regulatory standards and frameworks.
Requirements
- University degree in Life Sciences.
- 5+ years of experience in Regulatory Affairs, with a clear focus on medicinal products.
- Strong track record in EU regulatory procedures (NP, DCP, MRP) and variation management.
- Global experience (especially Middle East, Africa, Asia) is a strong plus.
- Fluent in English; French, Spanish or Arabic is a plus.
- Familiar with artwork processes and label compliance.
- Hands-on experience with regulatory systems (e.g. RIM, IDMP/SPOR).
- Strong communicator, structured, and comfortable working independently.
- Adaptable, proactive, and excited by cross-functional collaboration in a dynamic environment.
Ready to make your mark in a growing global company? Apply now and be part of the next chapter at Karo Healthcare.
Benefits
- Opportunity to create, grow, and encourage.
- Apart from a competitive salary pack, there are lots of growth opportunities to meet your personal ambitions.
- Flexible schedule, hybrid model with the primary workplace in the office, and life-work balance.
- Responsibility for exciting and challenging projects that have a direct, visible impact on our customers and the industry.
- Very positive work environment in a dynamic, international, and motivated team.
- Start-up spirit while being a part of the large international organization with strong values.
Karo Healthcare has a Diverse & Inclusive environment. We are looking for qualified candidates irrespective of gender, gender identity, sexual orientation, ethnicity, race, religion, national origin, disability or age.
Global Regulatory Affairs Manager employer: Karo Healthcare
Contact Detail:
Karo Healthcare Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Regulatory Affairs Manager
✨Tip Number 1
Familiarise yourself with Karo Healthcare's portfolio and their key brands. Understanding their products, especially in the medicinal category, will help you demonstrate your knowledge during discussions and show how you can contribute to their regulatory needs.
✨Tip Number 2
Network with professionals in the regulatory affairs field, particularly those with experience in EU procedures and global markets like the Middle East and Africa. Engaging with industry peers can provide insights and potentially lead to referrals.
✨Tip Number 3
Stay updated on the latest global regulatory standards and frameworks. Being well-informed about current trends and changes in regulations will position you as a knowledgeable candidate who can adapt quickly to evolving requirements.
✨Tip Number 4
Prepare to discuss your experience with cross-functional collaboration. Highlight specific examples where you've worked with different teams to achieve regulatory goals, as this role requires strong communication and teamwork skills.
We think you need these skills to ace Global Regulatory Affairs Manager
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Global Regulatory Affairs Manager position. Understand the key responsibilities and requirements, especially the focus on regulatory submissions for medicinal products.
Tailor Your CV: Customise your CV to highlight relevant experience in Regulatory Affairs, particularly your track record with EU regulatory procedures and any global experience you have. Emphasise your skills in managing regulatory submissions and cross-functional collaboration.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the company. Mention specific examples of how your background aligns with Karo Healthcare's mission and the responsibilities of the position. Highlight your adaptability and proactive approach.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a regulatory role.
How to prepare for a job interview at Karo Healthcare
✨Understand the Regulatory Landscape
Familiarise yourself with the latest global regulatory standards, especially those relevant to medicinal products. Being able to discuss recent changes or trends in regulations will demonstrate your expertise and commitment to staying informed.
✨Showcase Cross-Functional Collaboration
Prepare examples of how you've successfully collaborated with different teams in previous roles. Highlighting your ability to work cross-functionally will be crucial, as this role requires engaging with various departments and stakeholders.
✨Demonstrate Adaptability
Be ready to discuss situations where you've had to adapt quickly to changing regulations or project requirements. This role demands a proactive approach, so showcasing your flexibility will resonate well with the interviewers.
✨Prepare for Scenario-Based Questions
Anticipate questions that may ask you to solve hypothetical regulatory challenges. Practising your responses to these scenarios can help you articulate your problem-solving skills and strategic thinking effectively during the interview.
