Regulatory Affairs Support Specialist · RaySearch Laboratories AB (publ)

RaySearch develops innovative software solutions to improve cancer care. Over 1200 clinics in more than 54 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, Asia and Australia & New Zealand. Today we are more than 485 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.

As a Regulatory Affairs Support Specialist, you will join our Quality Assurance and Regulatory Affairs team of dedicated specialists working to ensure compliance with global medical device regulations and to bring innovative cancer treatment solutions to patients worldwide.

About the role

In this role, you will take ownership of RaySearch's regulatory vigilance activities and work closely with colleagues across Quality Assurance, Regulatory Affairs, Service, Development. You will be responsible for assessing, reporting and following up on vigilance cases, while also supporting regulatory submissions and registrations in global markets.

This is an excellent opportunity for someone with a few years of experience in medical device regulatory affairs who wants to deepen their expertise in vigilance and continue developing within global regulatory affairs.

The position is based at RaySearch's headquarters in Stockholm and reports to the Group Manager Regulatory.

Your main responsibilities:

Own and coordinate regulatory vigilance activities

Assess complaints and incidents for reportability under applicable regulations

Prepare, submit and follow up vigilance reports with competent authorities and notified bodies

Support post-market surveillance activities and regulatory compliance efforts

Support regulatory submissions and registrations in global markets

Maintain and update regulatory documentation and records

Monitor changes in regulatory requirements

Collaborate with internal stakeholders to ensure timely and compliant regulatory deliverables

Contribute to the continuous improvement of regulatory processes and procedures

Your profile

You are a positive, motivated and collaborative person with a genuine interest in regulatory affairs and medical devices. You enjoy taking responsibility, working in a structured way and finding practical solutions to complex regulatory challenges.

You are eager to learn, develop your expertise and grow within regulatory affairs. You thrive in a team environment, communicate effectively with different stakeholders and are comfortable managing multiple activities simultaneously while maintaining attention to detail.

Skills and experience:

University degree in Life Sciences, Engineering, Biomedical Engineering, or a related field

2 years of experience in regulatory affairs within the medical device industry

Experience working with EU MDR requirements

Experience working with ISO 13485

Experience with vigilance, complaint handling, post-market surveillance or related regulatory activities

Experience supporting regulatory submissions and registrations

Strong written and verbal communication skills in English

Ability to work independently and collaboratively in a cross-functional environment

Strong organizational skills and attention to detail

Merits:

Software as a medical device (SaMD)

Global regulatory submissions

FDA regulations and international regulatory frameworks

Radiation oncology

Our Culture

At RaySearch, we share a passion for innovation and the fight against cancer. Our team consists of dedicated experts who strive to deliver exceptional results through collaboration, attention to detail, and cutting-edge technology. We take pride in our role as a leader in cancer treatment, developing solutions that truly make a difference for patients worldwide.

Our Offer

We offer a dynamic and inclusive work environment in Hagastaden, Stockholm’s Life Science Hub. Our modern office space includes an in-house gym, yoga classes, and social activities such as after-work events. We also provide a fantastic lunch buffet, daily fika, and a stunning rooftop terrace with a 360-degree view of Stockholm. This comes with a competitive compensation and benefits package.

Application

Please apply for the position through the application form below. We do not accept applications via e-mail.