Hybrid-Work Regulatory Project Manager – Devices in London
Hybrid-Work Regulatory Project Manager – Devices

Hybrid-Work Regulatory Project Manager – Devices in London

London Full-Time 36000 - 60000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Manage global regulatory activities for drug-device combinations and ensure compliance.
  • Company: Leading pharmaceutical company focused on innovative patient solutions.
  • Benefits: Competitive salary, annual bonus, and flexible hybrid working model.
  • Why this job: Join a mission-driven team dedicated to improving patient outcomes globally.
  • Qualifications: Bachelor's in a scientific field and experience in regulatory affairs.
  • Other info: Dynamic work environment with opportunities for professional growth.

The predicted salary is between 36000 - 60000 £ per year.

A leading pharmaceutical company based in Greater London is seeking a CMC Regulatory Project Manager. This role involves managing regulatory activities for various drug-device combinations globally.

Candidates should have a Bachelor's in a scientific field and experience in regulatory affairs.

The position offers a competitive salary, annual bonus, and a flexible hybrid working model.

Join a team dedicated to improving patient outcomes with innovative solutions.

Hybrid-Work Regulatory Project Manager – Devices in London employer: Gsk

As a leading pharmaceutical company in Greater London, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee well-being and professional growth. With a competitive salary, annual bonuses, and a flexible hybrid working model, we empower our team to make a meaningful impact on patient outcomes while enjoying a supportive environment that encourages continuous learning and development.
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Contact Detail:

Gsk Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Hybrid-Work Regulatory Project Manager – Devices in London

Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical and regulatory fields on LinkedIn. Join relevant groups and engage in discussions to get your name out there.

Tip Number 2

Prepare for interviews by researching the company and its products. Understand their drug-device combinations and be ready to discuss how your experience aligns with their goals.

Tip Number 3

Showcase your skills! Create a portfolio or a presentation that highlights your past projects in regulatory affairs. This can set you apart from other candidates during interviews.

Tip Number 4

Don’t forget to apply through our website! We make it easy for you to find roles that match your skills and interests, so take advantage of it and get your application in!

We think you need these skills to ace Hybrid-Work Regulatory Project Manager – Devices in London

Regulatory Affairs
Project Management
Drug-Device Combination Knowledge
Scientific Background
Global Regulatory Compliance
Communication Skills
Team Collaboration
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs and any relevant scientific qualifications. We want to see how your background aligns with the role of a Regulatory Project Manager, so don’t hold back!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory activities and how you can contribute to improving patient outcomes. Keep it engaging and personal – we love to see your personality!

Showcase Your Experience: When detailing your past roles, focus on specific projects or achievements that relate to drug-device combinations. We’re looking for concrete examples that demonstrate your expertise and problem-solving skills in regulatory affairs.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!

How to prepare for a job interview at Gsk

Know Your Stuff

Make sure you brush up on your knowledge of regulatory affairs, especially in the context of drug-device combinations. Familiarise yourself with relevant regulations and guidelines that the company might be working with. This will show that you're not just interested in the role but also understand the complexities involved.

Showcase Your Experience

Prepare to discuss your previous experience in regulatory project management. Have specific examples ready that highlight your achievements and how they relate to the job description. This is your chance to demonstrate how your background aligns with their needs.

Ask Insightful Questions

Come prepared with questions that show your interest in the company and the role. Ask about their current projects or challenges they face in regulatory affairs. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.

Embrace the Hybrid Model

Since this role offers a flexible hybrid working model, be ready to discuss how you manage your time and productivity in both remote and in-office settings. Share any strategies you've used to stay organised and effective while working in a hybrid environment.

Hybrid-Work Regulatory Project Manager – Devices in London
Gsk
Location: London
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  • Hybrid-Work Regulatory Project Manager – Devices in London

    London
    Full-Time
    36000 - 60000 £ / year (est.)
  • G

    Gsk

    10000+
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