- Lön
- Ej angiven
- Distans
- Hybrid
- Senioritet
- Senior
- svenska
- Ej angivet
- Arbetstillstånd eller flytt
- Nämns inte
- Anställning
- Heltid · 12 månader – upp till 2 år
- Publicerad
- 29 juni 2026
- Sista ansökningsdag
- 12 nov. 2026
- Tjänster
- 3
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Kort om jobbet
Detta är en tjänst som Global Regulatory Specialist hos Celsus Engineering AB i Stockholm. Tjänsten täcker efterlevnad för medicintekniska produkter med krav på minst fem års erfarenhet inom området.
Kompetenser i annonsen
Originalannons
About the Role
As a Global Regulatory Specialist, you will join our Quality & Regulatory Affairs team to help ensure our medical devices and mounting systems meet global regulatory requirements.
Please note: This is a hybrid role with 1–3 days per week onsite at our Stockholm office in Östermalm, especially during onboarding. Occasional international travel (10–20%) may be required and will be communicated in advance.
In this role you will:
Streamline regulatory processes and set a roadmap in collaboration Product & Development, QA, and Operations teams.
Coordinate with internal and external auditors to support audit readiness.
Review device classifications and regulatory challenges across markets.
Maintain and update technical documentation (Annex II & III) and declarations of conformity, including EU Declaration of Conformity, in alignment with the associated technical documentation.
Coordinate establishment of registrations and device listings with the FDA, Authorized Representatives, and Importers/Distributors.
Support product registrations and market access activities (EU MDR Class I, FDA 510(k)-exempt Class II).
Monitor regulatory changes and communicate implications to relevant teams.
What We’re Looking For
We are looking for a structured and collaborative regulatory professional who enjoys solving problems with a logical approach, works autonomously while contributing to strategic initiatives, and thrives in a dynamic, cross-functional environment.
We’re looking for a detail-oriented and analytical professional with:
A bachelor’s degree in Regulatory Affairs, Life Sciences, Electrical-Electronics or a related field.
At least 5 years of experience in medical device regulatory affairs with hands-on experience with EU MDR (Class I) and FDA QSR.
Experience with regulatory systems, document control tools, and QMS platforms and exposure to technical documentation, internal and external audits for regulatory compliance
Strong organization, coordination and communication skills to engage auditors and communicating with stakeholders across functions and levels.
Ability to break down complex regulatory topics clearly for both technical and non-technical stakeholders.
Proficiency in both spoken and written communication in English.
Ideal candidates will bring:
Familiarity with embedded systems and experience with IEC 62304.
Experience with EU MDR (Class II/III).
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