At a Glance
- Tasks: Support the development and registration of innovative solid tumour products across EMEA.
- Company: Join a leading pharmaceutical company dedicated to advancing healthcare.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with strong focus on career development and cross-functional teamwork.
- Why this job: Make a real impact in healthcare by shaping regulatory strategies for groundbreaking treatments.
- Qualifications: Bachelor's degree in life sciences and 2+ years of regulatory experience required.
The predicted salary is between 50000 - 70000 £ per year.
EMEA Regulatory Affairs Solid Tumours is recruiting for a dedicated Experienced Regulatory Affairs Professional to work on the development and registration of solid tumour products in Europe, the Middle East, and Africa (EMEA). The Regulatory Affairs Professional supports the development, registration, and lifecycle management of pharmaceutical products within the EMEA region. This role focuses on regulatory tasks such as submission strategies, procedural aspects of regulatory affairs, and compliance with applicable health authority (HA) regulations, project management, and would support the EMEA regulatory leader on regulatory product strategy.
The position can be based in Belgium, The Netherlands, Poland or the United Kingdom. This is a hybrid role, meaning regular office presence is required in coordination with your team. This role provides an opportunity to support small and large molecules, and in different oncology indications, contributing to advancements in healthcare. The successful applicant will help develop and implement regulatory strategies to achieve efficient development and timely commercialization of innovative pharmaceutical products in compliance with applicable regulations.
General Regulatory Responsibilities- Guide project teams on regulatory requirements and contribute to regional and local regulatory strategies.
- Support the EMEA Regulatory Leader in developing regulatory strategies for products in product development.
- Assist in submissions to health authorities, including CTAs, MAAs, and lifecycle submissions.
- Contribute to Global Regulatory and cross-functional meetings as the EMEA Regulatory Professional.
- Develop an understanding of the regional regulatory environment, therapeutic area, and competitor intelligence.
- Draft and review document content based on regulatory knowledge.
- Review clinical trial protocols to ensure alignment with regulatory requirements.
- Provide guidance on CTA submission strategies and documents such as protocols and Investigator’s Brochures (IB).
- Coordinate responses to Health Authority Questions (HAQs).
- Contribute to the development of regulatory submission documents such as briefing documents, Paediatric Investigational Plans (PIPs), and Orphan Drug Designations.
- Review response documents to ensure they thoroughly and accurately address regulatory questions.
- Provide regulatory support to the EMEA Regulatory Leader throughout the product lifecycle.
- Guide and collaborate with cross-functional teams on required documents and submission strategies for MAA preparation.
- Identify and supervise critical path activities.
- Assist with timely submission and acceptance of MAA and subsequent procedural steps.
- Ensure country-specific submission packages are made available to Local Operating Companies (LOCs) in accordance with agreed plans.
- Support lifecycle submissions and post-approval regulatory activities including Variations, Post-marketing Commitments and Safety related submissions.
- Maintain oversight of regional lifecycle submissions.
- Act as backup for contact with EMA and national Regulatory Agencies.
- Support the preparation of meetings with Regulatory Agencies.
- Collaborate with LOCs, informing regarding product and development status, addressing queries as appropriate.
- Assist in the creation and revision of processes related to regulatory submissions.
- Appropriately manage Regulatory Affairs related systems and processes according to regulatory and company standards.
- Bachelor’s degree (BS) in life sciences, medical, or paramedical fields (e.g., pharmacy, biology, veterinary science), or equivalent experience.
- A Master’s degree (MS), MBA, or higher qualification is considered a plus.
- Experience in pharmaceutical industry or similar and / or Regulatory Affairs.
- 2 or more years of regulatory experience, capable of working independently on key tasks while escalating higher-complexity issues.
- Experience working in cross-functional teams.
- Strong oral & written communication skills in English.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to follow local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).
Experienced Regulatory Affairs Professional EMEA employer: meeveem
As an employer, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make meaningful contributions to healthcare advancements. With a strong focus on professional development, we offer extensive growth opportunities and support for our team members in the EMEA region, ensuring they thrive in their roles while working on cutting-edge pharmaceutical products. Our hybrid work model allows for flexibility, making it easier to balance personal and professional commitments while being part of a dedicated team committed to excellence.
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We think this is how you could land Experienced Regulatory Affairs Professional EMEA
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We think you need these skills to ace Experienced Regulatory Affairs Professional EMEA
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at meeveem!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show meeveem that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at meeveem!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At meeveem, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at meeveem
✨Understand the Science
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 meeveem that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with meeveem’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
