Regulatory Affairs Specialist
Elekta
Date: 13 hours ago
City: Crawley, England
Contract type: Full time
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
You are detail-oriented, organized, and proactive. You thrive in cross-functional settings and are passionate about compliance and operational excellence.
You bring expertise in regulatory operations and a passion for contributing to high-quality healthcare solutions.
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.
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 [email protected]. 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.
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.
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.
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.
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
- 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)
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 [email protected]. 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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