Regulatory Affairs Specialist
Regulatory Affairs Specialist

Regulatory Affairs Specialist

Crawley Full-Time 28800 - 48000 ÂŁ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Ensure our products meet regulatory requirements while enabling efficient order processing and delivery.
  • Company: Elekta is a leader in precision radiation therapy, dedicated to improving cancer care worldwide.
  • Benefits: Enjoy hybrid work options, up to 25 paid vacation days, private medical insurance, and more!
  • Why this job: Join a mission-driven team that builds hope for cancer patients globally through innovative technology.
  • Qualifications: Experience in regulatory affairs or operations, strong organisational skills, and a passion for healthcare solutions.
  • Other info: We welcome unique skills and experiences—apply even if you don’t meet every requirement!

The predicted salary is between 28800 - 48000 ÂŁ per year.

Are you a current Elekta employee?

Please click here to apply through our internal career site Find Jobs – Elekta .

Want to join a team with a mission to improve and save lives?

We continually look for motivated and skilled individuals who are interested in supporting our customers – healthcare professionals who use our products to help patients and their communities.

We currently have the following opportunity available – please contact us for more details!

We don’t just build technology. We build hope for everyone dealing with cancer.

What you’ll do at Elekta

At Elekta, we don’t just build technology—we build hope for everyone dealing with cancer. As a Regulatory Specialist, you will play a critical role in ensuring our products meet regulatory requirements while enabling efficient order processing and delivery. Your work will directly impact how we serve hospitals, clinicians, and patients worldwide by maintaining compliance without compromising delivery timelines.

You will collaborate with stakeholders across Regulatory Affairs, Product Management, Order Handling, Logistics, and other key teams to manage regulatory block and release processes for products and spare parts. Your focus will be on process efficiency, compliance, and continuous improvement.

Responsibilities

  • Maintain and update the Regulatory Release Matrix to reflect new product registrations and releases.

  • Provide regulatory input for the catalogue and ensure catalogue accuracy against registrations; act as the main RA contact for the catalogue team.

  • Represent Regulatory Affairs in Order Process reviews and support unblocking activities.

  • Coordinate block and release activities to meet operational KPIs.

  • Drive process improvements and implement changes to enhance the block & release process.

  • Provide timely and accurate information to support order and spare part release decisions.

  • Report on process performance and update blocked/unblocked product status weekly.

  • Review RA Release Forecasts, identify potential issues, and propose corrective actions.

  • Support other tasks as assigned by your manager.

The right stuff

You are detail-oriented, organized, and proactive. You thrive in cross-functional settings and are passionate about compliance and operational excellence.

  • Strong communication and coordination skills across multiple teams.

  • Analytical mindset with a focus on process improvement.

  • Ability to work under pressure and meet tight deadlines.

  • A collaborative approach and a drive to find solutions.

What you bring

You bring expertise in regulatory operations and a passion for contributing to high-quality healthcare solutions.

  • Experience in regulatory affairs, operations, or order fulfillment processes (MedTech preferred).

  • Ability to interpret and apply regulatory requirements in operational processes.

  • Strong organizational and data management skills.

  • Experience working in matrixed or cross-functional teams.

  • Proficiency with ERP systems (e.g., M3) and regulatory tracking tools.

We encourage you to apply even if you don’t meet every requirement—your unique skills and experiences might be exactly what we\’re looking for!

What you’ll get

In this role, you will work for a higher purpose — hope for everyone dealing with cancer, and for everyone, regardless of where they are in the world, to have access to the best cancer care. You will be part of a collaborative, global team committed to delivering innovation and excellence.

In this role, you will work for a higher purpose; hope for everyone dealing with cancer,

and for everyone regardless of where in the world, to have access to the best cancer

care. In addition to this, Elekta offers a range of benefits.

• Hybrid work option (you are required to work from the Crawley HQ at least 3

days/week)

• Up to 25 paid vacation days (plus bank holidays)

• Holiday Purchase Scheme

• Private Medical Insurance

• Attractive Employer Pension Contribution Package

• Cycle to work scheme

• Life Assurance

• Onsite subsidized restaurant, offering budget-friendly dining

• Love electric (Electric vehicle salary sacrifice scheme)

Hiring process

We look forward to hearing from you! Apply by submitting your application and résumé in English via the “Apply” button. Please note that we do not accept applications via e-mail.

Your Elekta contact

For questions, please contact the Global Talent Acquisition Partner responsible, Gustaf Ericson, at . We do not accept applications through e-mail.

We are an equal opportunity employer

We are an equal opportunity employer. We evaluate qualified applicants without regard to age, race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, disability, veteran status, or any other protected characteristic.

About Elekta

As a leader in precision radiation therapy, Elekta is committed to ensuring every patient has access to the best cancer care possible. Elekta is a proud innovator and supplier of equipment and software used to improve, prolong, and save the lives of people with cancer and brain disorders.

More than 6,000 hospitals worldwide rely on Elekta technology. We openly collaborate with customers to advance sustainable, outcome-driven, and cost-efficient solutions to meet evolving patient needs, improve lives, and bring hope to everyone dealing with cancer. To us, it’s personal, and our global team of 4,700 employees combines passion, science, and imagination to profoundly change cancer care. We don’t just build technology, we build hope.

Elekta is headquartered in Stockholm, Sweden, with a presence in more than 120 countries and listed on Nasdaq Stockholm. For more information, visit elekta.com or follow @Elekta on LinkedIn and Twitter.

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Regulatory Affairs Specialist employer: Elekta

Elekta is an exceptional employer dedicated to improving and saving lives through innovative cancer care solutions. With a collaborative work culture and a strong commitment to employee growth, we offer a hybrid work model, generous vacation days, and comprehensive benefits including private medical insurance and a robust pension plan. Join us at our Crawley HQ, where your contributions will directly impact healthcare professionals and patients worldwide, fostering a sense of purpose and community.
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Contact Detail:

Elekta Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Affairs Specialist

✨Tip Number 1

Familiarise yourself with the regulatory landscape specific to MedTech. Understanding the key regulations and compliance requirements will not only help you in interviews but also demonstrate your commitment to the role.

✨Tip Number 2

Network with current or former employees of Elekta, especially those in Regulatory Affairs. They can provide valuable insights into the company culture and expectations, which can be a game-changer during your application process.

✨Tip Number 3

Prepare to discuss specific examples of how you've improved processes in previous roles. Elekta values operational excellence, so showcasing your analytical mindset and problem-solving skills will set you apart.

✨Tip Number 4

Stay updated on the latest trends and technologies in cancer care and regulatory affairs. Being knowledgeable about current advancements will show your passion for the field and your readiness to contribute to Elekta's mission.

We think you need these skills to ace Regulatory Affairs Specialist

Regulatory Affairs Expertise
Attention to Detail
Process Improvement
Data Management Skills
Analytical Skills
Strong Communication Skills
Cross-Functional Collaboration
Organisational Skills
Ability to Work Under Pressure
Proficiency with ERP Systems (e.g., M3)
Regulatory Tracking Tools Experience
Operational Excellence
Problem-Solving Skills
Timely Reporting and Documentation

Some tips for your application 🫡

Understand the Role: Before applying, make sure to thoroughly read the job description for the Regulatory Affairs Specialist position. Understand the key responsibilities and required skills, as this will help you tailor your application effectively.

Tailor Your CV: Customise your CV to highlight relevant experience in regulatory affairs, operations, or order fulfilment processes. Emphasise your analytical mindset and any experience with ERP systems or regulatory tracking tools, as these are crucial for the role.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for compliance and operational excellence. Mention specific examples of how you've contributed to process improvements in previous roles, and express your enthusiasm for Elekta's mission to improve cancer care.

Follow Application Instructions: Ensure you submit your application through the designated 'Apply' button on the Elekta website. Double-check that all documents are in English and that you have included your résumé and any other required materials. Remember, applications via email are not accepted.

How to prepare for a job interview at Elekta

✨Understand Regulatory Requirements

Familiarise yourself with the specific regulatory requirements relevant to the MedTech industry. Be prepared to discuss how you have previously interpreted and applied these regulations in your work.

✨Showcase Your Analytical Skills

Highlight your analytical mindset by discussing past experiences where you identified process inefficiencies and proposed improvements. Use specific examples to demonstrate your problem-solving abilities.

✨Emphasise Cross-Functional Collaboration

Since the role involves working with various teams, be ready to share examples of how you've successfully collaborated across departments. This will show your ability to thrive in a matrixed environment.

✨Prepare for Scenario-Based Questions

Anticipate scenario-based questions that may assess your ability to handle regulatory blocks or compliance issues. Think through your responses and consider how you would approach these challenges in a real-world context.

Regulatory Affairs Specialist
Elekta
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  • Regulatory Affairs Specialist

    Crawley
    Full-Time
    28800 - 48000 ÂŁ / year (est.)

    Application deadline: 2027-07-16

  • E

    Elekta

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