Docuvera Regulatory Specialist — Submissions & Compliance in London
Docuvera Regulatory Specialist — Submissions & Compliance

Docuvera Regulatory Specialist — Submissions & Compliance in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Create and manage regulatory documents while ensuring compliance with industry standards.
  • Company: Join a dynamic recruitment agency supporting GSK in the pharmaceutical sector.
  • Benefits: Enjoy a hybrid work model with competitive pay and professional growth opportunities.
  • Why this job: Make a real impact in regulatory affairs and collaborate with diverse teams.
  • Qualifications: Experience with Docuvera in a pharmaceutical setting is essential.
  • Other info: Focus on quality and compliance in a supportive environment.

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

A recruitment agency is seeking a Docuvera Specialist for Regulatory Affairs support. The role requires experience with Docuvera in a pharmaceutical setting and involves creating and managing regulatory documents.

Key responsibilities include:

  • Ensuring compliance with regulatory standards
  • Collaborating with various teams

This position is hybrid and based in the UK, supporting GSK indirectly through a partner organization, which entails a strong focus on quality and regulatory compliance.

Docuvera Regulatory Specialist — Submissions & Compliance in London employer: Harrington Recruitment

As a Docuvera Regulatory Specialist at our partner organisation, you will thrive in a dynamic hybrid work environment that champions quality and compliance in the pharmaceutical sector. We offer a supportive culture that prioritises employee growth through continuous training and development opportunities, ensuring you can advance your career while making a meaningful impact on regulatory affairs. Join us in the UK, where your expertise will be valued, and your contributions will help shape the future of healthcare.
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Contact Detail:

Harrington Recruitment Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Docuvera Regulatory Specialist — Submissions & Compliance in London

Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field, especially those who have experience with Docuvera. A friendly chat can open doors and give you insights that might just land you that interview.

Tip Number 2

Prepare for the interview by brushing up on your knowledge of regulatory compliance standards. We want you to be able to discuss how your experience aligns with the role's requirements, so practice articulating your past achievements in this area.

Tip Number 3

Showcase your collaborative spirit! Since the role involves working with various teams, think of examples where you've successfully collaborated in the past. We want to see how you can contribute to a team environment.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate candidates who are ready to make an impact in the regulatory space.

We think you need these skills to ace Docuvera Regulatory Specialist — Submissions & Compliance in London

Docuvera
Regulatory Affairs
Regulatory Compliance
Document Management
Collaboration Skills
Quality Assurance
Pharmaceutical Knowledge
Attention to Detail

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience with Docuvera and regulatory affairs. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory compliance and how your background makes you a perfect fit for the Docuvera Specialist role. Let us know what excites you about working with GSK!

Showcase Collaboration Skills: Since this role involves working with various teams, highlight any past experiences where you’ve successfully collaborated. We love to see examples of teamwork and how you’ve contributed to achieving compliance goals.

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

How to prepare for a job interview at Harrington Recruitment

Know Your Docuvera Inside Out

Make sure you’re well-versed in Docuvera and its applications in regulatory affairs. Brush up on your experience with creating and managing regulatory documents, as this will likely come up during the interview. Be ready to discuss specific examples of how you've ensured compliance in previous roles.

Understand Regulatory Standards

Familiarise yourself with the key regulatory standards relevant to the pharmaceutical industry. This knowledge will not only help you answer questions confidently but also demonstrate your commitment to quality and compliance. Consider preparing a few insights on how these standards impact document management.

Collaboration is Key

Since the role involves working with various teams, think about your past experiences collaborating across departments. Prepare to share examples that highlight your teamwork skills and how you’ve successfully navigated challenges in a hybrid work environment.

Ask Insightful Questions

Prepare thoughtful questions to ask at the end of your interview. This shows your genuine interest in the role and the company. You might want to inquire about the team dynamics or how they measure success in regulatory compliance, which can give you valuable insights into their expectations.

Docuvera Regulatory Specialist — Submissions & Compliance in London
Harrington Recruitment
Location: London

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