Regulatory Lead - Medical Device Software
RaySearch Laboratories AB (publ)Sammanfattning
RaySearch is seeking a Regulatory Lead to oversee the regulatory strategy and lifecycle for one of its medical device software products. This role involves collaboration with various teams to ensure compliance and drive market access. The position is based in Hagastaden, Stockholm, within a company dedicated to improving cancer care through innovative solutions.Jobbet i korthet
Anställningstyp
tillsvidareanstallning
Arbetstid
heltid
Förmåner
Diverse and inclusive work environment.Modern workspace with an in-house gym and social activities.Daily morning and afternoon fika.Competitive compensation and benefits package.Stunning rooftop terrace with a 360-degree view of Stockholm.
Ansök senast: 2026-08-29
Publicerad: 2026-07-10
Beskrivning
RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination.
Are you a driven regulatory professional who enjoys ownership, collaboration and working close to product development? This could be the role for you. Apply and help shape the future of medical device software at RaySearch.About the role
We are looking for an experienced and driven Regulatory Lead to own the regulatory strategy and lifecycle oversight for one of RaySearch's products. In this role, you will be the regulatory point of contact for the product, working closely with key stakeholders in the Development, Corporate Strategy and Sales teams. You will help shape product strategy, guide development activities, drive market access, and ensure compliance throughout the product lifecycle.
This is a highly visible role for someone who enjoys combining deep regulatory expertise with strategic thinking, project coordination, and collaboration across the organization.
What you'll do
Own and drive the global regulatory strategy for your product throughout its lifecycle.
Lead the preparation, review, and maintenance of Technical Documentation and regulatory submissions, including EU MDR.
Act as the regulatory expert within development projects and ensure regulatory requirements are integrated throughout the design and development process.
Coordinate and oversee multiple projects, priorities, and submission timelines while maintaining a long-term view of the product roadmap.
Partner closely with Development, Corporate Strategy, Sales and other key stakeholders to support product development and market access.
Support inspections, audits, post-market activities, and continuous improvements.
Your profile
You are a proactive and pragmatic regulatory professional who enjoys taking ownership and driving things forward. You are technically strong, comfortable working with development teams, and able to translate complex regulatory requirements into practical solutions.
You like having oversight of the full product picture-from early development and regulatory strategy to submission and post-market activities-and you thrive in a collaborative, fast-paced environment where you can make a real impact.
Requirements
Bachelor's or Master's degree in Engineering, Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field.
Several years of Regulatory Affairs experience within the medical device industry.
Strong experience preparing and reviewing Technical Documentation under EU MDR.
Experience working with medical device product development and design control processes.
Experience with medical device software
Strong knowledge of IEC 62304, IEC 60601 and ISO 14971
Strong project management and stakeholder management skills.
Ability to manage multiple activities and timelines while maintaining the bigger picture.
Proficiency in English.
Meriting experience
US regulatory experience, Experience with FDA submissions, including eSTAR/510(k).
Experience with IEC 62366 and ISO 14155
Experience with Cybersecurity requirements for medical devices.
Experience with AI/ML-enabled medical devices.
Our Culture
Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care.
Our Offer
At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package.
Application
Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.
Are you a driven regulatory professional who enjoys ownership, collaboration and working close to product development? This could be the role for you. Apply and help shape the future of medical device software at RaySearch.About the role
We are looking for an experienced and driven Regulatory Lead to own the regulatory strategy and lifecycle oversight for one of RaySearch's products. In this role, you will be the regulatory point of contact for the product, working closely with key stakeholders in the Development, Corporate Strategy and Sales teams. You will help shape product strategy, guide development activities, drive market access, and ensure compliance throughout the product lifecycle.
This is a highly visible role for someone who enjoys combining deep regulatory expertise with strategic thinking, project coordination, and collaboration across the organization.
What you'll do
Own and drive the global regulatory strategy for your product throughout its lifecycle.
Lead the preparation, review, and maintenance of Technical Documentation and regulatory submissions, including EU MDR.
Act as the regulatory expert within development projects and ensure regulatory requirements are integrated throughout the design and development process.
Coordinate and oversee multiple projects, priorities, and submission timelines while maintaining a long-term view of the product roadmap.
Partner closely with Development, Corporate Strategy, Sales and other key stakeholders to support product development and market access.
Support inspections, audits, post-market activities, and continuous improvements.
Your profile
You are a proactive and pragmatic regulatory professional who enjoys taking ownership and driving things forward. You are technically strong, comfortable working with development teams, and able to translate complex regulatory requirements into practical solutions.
You like having oversight of the full product picture-from early development and regulatory strategy to submission and post-market activities-and you thrive in a collaborative, fast-paced environment where you can make a real impact.
Requirements
Bachelor's or Master's degree in Engineering, Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field.
Several years of Regulatory Affairs experience within the medical device industry.
Strong experience preparing and reviewing Technical Documentation under EU MDR.
Experience working with medical device product development and design control processes.
Experience with medical device software
Strong knowledge of IEC 62304, IEC 60601 and ISO 14971
Strong project management and stakeholder management skills.
Ability to manage multiple activities and timelines while maintaining the bigger picture.
Proficiency in English.
Meriting experience
US regulatory experience, Experience with FDA submissions, including eSTAR/510(k).
Experience with IEC 62366 and ISO 14155
Experience with Cybersecurity requirements for medical devices.
Experience with AI/ML-enabled medical devices.
Our Culture
Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care.
Our Offer
At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package.
Application
Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.
Ansök till tjänsten
Regulatory Lead - Medical Device Software
OM FÖRETAGET
RaySearch Laboratories AB (publ)
