The opportunity:
In this role, you will dive into a dynamic industry that actively collaborates across the Pharmaceutical, Medical Device, and Tech sectors. As a vital member of our team, you will collaborate closely with experts across the entire organization. We are seeking a dedicated and skilled Compliance Specialist to join our team. The successful candidate will play a critical role in driving the our organization’s information security and privacy efforts by implementing and maintaining robust procedures. You will enjoy a high degree of freedom to influence your daily work and contribute to the overall development of the company.
Note: This is a fixed-term position lasting until 18 May 2027, with the possibility of extension. We are looking to hire as soon as possible, following due process
What you’ll do:
- Drive, maintain and ensure effectiveness of the data protection and information security policies, procedures and controls across the organization
- Conduct relevant assessments (such as data protection impact assessment and supplier assessments) and maintain documentation (such as record for processing activities and retention schedules)
- Be the point of contact for implementation of privacy-by-design during product development
- Provide regulatory input on data protection and information security requirements for going to new markets
- Ensure traceability of implementation of date protection and information security efforts and participate in audit
About you:
- You are driven by the same purpose as us and want to contribute to improving the lives of patients around the world
- You have a positive and curious minds
- You understand how to balance quality and pragmatism to ensure the best possible outcome for a given project
- You are looking for a fun, friendly, and tolerant working environment in a purpose-driven company where your opinion matters
- You have 1-3 years of experience working with information security and data protection compliance
- You have relevant privacy or security certification
- You strive to handle a wide range of tasks in a dynamic environment
- You have a relevant educational background
- You have professional proficiency in English
Nices to haves - bonus points:
- Experience working with Software as a Medical Device (SaMD) or digital products
- Experience with standards and regulations like: ISO 13485, GxP, ISO27001, GDPR
- Participated in audits
What we offer:
- A portfolio of meaningful products that impact patient lives at scale.
- Autonomy, trust, and support to do the best work of your career.
- An open, collaborative environment with talented peers across engineering, design, clinical, and regulatory.
- Career growth in one of the leading digital health scale-ups, alongside world-class pharma partners.
- The opportunity to leave your mark on the future of digital health.
- Copenhagen’s best view and best office espresso machine ☕️
