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- Tasks: Lead global regulatory submissions for medicinal products and collaborate across functions.
- Company: Karo Healthcare is a dynamic personal-care retail company with a diverse portfolio in 90 countries.
- Benefits: Enjoy a flexible schedule, hybrid work model, and numerous growth opportunities.
- 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 of Regulatory Affairs experience required.
- Other info: Karo Healthcare values diversity and inclusivity, welcoming candidates from all backgrounds.
The predicted salary is between 36000 - 60000 £ 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 portfolio includes such brands as E45, Pevaryl, Lamisil, Nutravita, Decubal and many others. 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\’re 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
In this role, you’ll lead global regulatory submissions for our medicinal products and serve as a strategic partner across functions. You’ll work independently, adapt quickly, and contribute with a strong understanding of how regulatory work drives broader business outcomes.
- 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
- 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.
- 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 work place 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.
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Global Regulatory Affairs Manager employer: Karo Group, Inc.
Contact Detail:
Karo Group, Inc. 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 who have experience in global markets like the Middle East, Africa, and Asia. Engaging with industry peers can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Stay updated on the latest global regulatory standards and frameworks relevant to medicinal products. This knowledge will not only prepare you for the role but also demonstrate your commitment to continuous learning and adaptability.
✨Tip Number 4
Prepare to discuss your experience with regulatory systems like RIM and IDMP/SPOR. Being able to articulate your hands-on experience with these tools will set you apart as a candidate who can hit the ground running.
We think you need these skills to ace Global Regulatory Affairs Manager
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Global Regulatory Affairs Manager position. Tailor your application to highlight your relevant experience in regulatory affairs, especially with medicinal products.
Highlight Relevant Experience: In your CV and cover letter, emphasise your 5+ years of experience in Regulatory Affairs, particularly your familiarity with EU regulatory procedures and any global experience you have, especially in the Middle East, Africa, and Asia.
Showcase Communication Skills: As a strong communicator is essential for this role, provide examples in your application that demonstrate your ability to collaborate cross-functionally and manage relationships with various stakeholders.
Tailor Your Cover Letter: Craft a compelling cover letter that not only outlines your qualifications but also reflects your enthusiasm for Karo Healthcare's mission and values. Mention how you can contribute to their growth strategy and adapt to their dynamic environment.
How to prepare for a job interview at Karo Group, Inc.
✨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 the role.
✨Showcase Cross-Functional Collaboration
Prepare examples of how you've successfully collaborated with different teams in previous roles. Highlighting your ability to work independently while also engaging with diverse functions will resonate well with the interviewers.
✨Demonstrate Adaptability
Be ready to discuss situations where you had to adapt quickly to changing regulations or project requirements. This role requires a proactive approach, so showcasing your flexibility will be key.
✨Highlight Your Global Experience
If you have experience working in or with markets in the Middle East, Africa, or Asia, make sure to bring this up. Discussing specific projects or challenges you've faced in these regions can set you apart from other candidates.
