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- Tasks: Lead regulatory strategies for innovative medicines in Europe and globally.
- Company: Join Teva, a leader in healthcare innovation with a focus on growth.
- Benefits: Enjoy hybrid work, 25 days leave, health insurance, and wellness programs.
- Why this job: Be part of a dynamic team impacting global health with innovative products.
- Qualifications: Must have a BSc in Life Sciences and substantial European regulatory experience.
- Other info: Located near London, with a strong focus on employee well-being and development.
The predicted salary is between 43200 - 72000 £ per year.
to work within the Global Regulatory Affairs – Innovative Medicines (Europe) team. You will be working with key
Innovative products
part of Teva’s Pivot to Growth strategy.
Do you know that our Harlow office is the Centre of Excellence (CoE) for Regulatory Affairs within Teva, with teams covering both European and global licensing for medicines and over-the-counter (OTC) products? The site is conveniently located half an hour commute from central London.
We have a hybrid approach to home working!
A day in the life of a Manager/Senior Manager Regulatory Affairs…
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You will develop regulatory strategies during development, approval and post approval phases for submissions to EU Competent Authorities. Depending on your experience you may also have the opportunity to do this on a Global scale in the capacity of Global Regulatory Lead.
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You will obtain regulatory approvals and other feed-back or decisions from European Competent Authorities during development of innovative medicinal products.
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You will support Clinical Trial Applications under the new Clinical Trials Regulation.
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You will obtain registrations for innovative medicinal products, in the EU and to ensure that the registrations for existing marketed products are maintained.
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You will provide regulatory guidance to cross-functional teams within Teva.
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A strong Scientific background with a BSc degree in Life or Pharmaceutical/Healthcare Sciences – ideally with a MSc or PhD
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Substantial European regulatory affairs experience (must have)
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Experience in Clinical Trial Applications in the EU (must have)
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Innovative Medicine experience
in Immunology and/or Oncology and/or Gastroenterology and/or Respiratory
therapeutic areas is a significant advantage, but we are open to consider any therapeutic area
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Experience with Medical Devices and the Medical Device Regulation would also be an advantage
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Strong leadership and interpersonal skills
Are you?
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An excellent written and verbal communicator and confident presenting/communicating with local and global groups
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Able to work under pressure to meet tight deadlines
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A strategic thinker with strong problem solving skills
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Enjoying time with your families (25 days of annual leave, Hybrid approach to home working, Pension scheme, car or car allowance)
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Looking after your health (Life & Critical Illness Insurance, Private health insurance for you and your family, Sports and Health Programme – including health days and nutritional counselling, On-site Canteen)
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Recognizing your value (Recognition programs to reward our employees with our company bonus scheme)
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Boosting your potential (Virtual Learning Centre)
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Well-being and D&I focused company
Manager - Regulatory Affairs - Innovative Medicines, Europe employer: Teva Pharmaceuticals
Contact Detail:
Teva Pharmaceuticals Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager - Regulatory Affairs - Innovative Medicines, Europe
✨Tip Number 1
Familiarize yourself with the latest EU regulations and guidelines related to innovative medicines. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the regulatory affairs space, especially those who have experience with Teva or similar companies. Engaging with them on platforms like LinkedIn can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that showcase your ability to develop regulatory strategies and manage submissions. Highlight any successful projects, particularly in the therapeutic areas mentioned in the job description.
✨Tip Number 4
Research Teva's Pivot to Growth strategy and be ready to articulate how your background aligns with their goals. Showing that you understand their vision will set you apart as a candidate who is genuinely interested in contributing to their success.
We think you need these skills to ace Manager - Regulatory Affairs - Innovative Medicines, Europe
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and requirements. Highlight your relevant experience in regulatory affairs, especially in innovative medicines and clinical trial applications.
Tailor Your CV: Customize your CV to reflect your experience in European regulatory affairs and any specific therapeutic areas mentioned in the job description. Emphasize your leadership skills and ability to work under pressure.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory affairs and your strategic thinking abilities. Mention how your background aligns with Teva's Pivot to Growth strategy and your interest in contributing to their innovative products.
Highlight Communication Skills: Since excellent communication is crucial for this role, provide examples in your application of how you've effectively communicated with cross-functional teams or presented to stakeholders in the past.
How to prepare for a job interview at Teva Pharmaceuticals
✨Showcase Your Regulatory Expertise
Make sure to highlight your substantial experience in European regulatory affairs. Be prepared to discuss specific examples of how you've developed regulatory strategies and obtained approvals from EU Competent Authorities.
✨Demonstrate Your Scientific Background
Since a strong scientific background is crucial for this role, be ready to talk about your educational qualifications and any relevant research or projects you've been involved in, especially in innovative medicines.
✨Communicate Effectively
As an excellent communicator, you should practice articulating complex regulatory concepts clearly and confidently. Prepare to present your ideas and experiences in a way that resonates with both local and global teams.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to work under pressure. Think of scenarios where you've successfully navigated tight deadlines or complex regulatory challenges, and be ready to share those stories.
