20 bästa jobben som regulatory compliance i malmö (Rekryterar nu!)

Hands-on Regulatory Affairs Expert
Sunmedic AB —Vellinge
- Heltid
- Engelska
- Masterexamen
- Kandidatexamen
Regulatory Affairs Associate
Agardh Recruitment & Consulting —Höllviken
- Spanska
- Engelska
- Projektledning
Sustainability Compliance & Reporting Intern
AAK International —Malmö
- Microsoft Excel
- Engelska
- Microsoft Office
Junior Kvalitetskonsult (Life Science)
Capgemini Sogeti —Malmö
Compliance & Validation Specialist
PolyPeptide Group —Malmö
- Engelska
- Masterexamen
- Kandidatexamen
Senior Regulatory Affairs Manager - Camurus (Lund)
TOBLOR Consulting AB —Lund
- Heltid
- Engelska
- Masterexamen
- Projektledning
11d
Junior Kvalitetskonsult (Life Science)
Capgemini Sweden —Malmö
Financial Controller
AAK International —Malmö
- Microsoft Excel
- Oracle
- Engelska
Senior Product Manager
Tunstall Sweden —Malmö
- Microsoft Word
- Microsoft Excel
- Personalansvar
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Sr. Project Manager – R&D
Nipro Europe Group Companies —Malmö
- Kontor
- Masterexamen
- Projektledning
Senior Regulatory Affairs Manager - Camurus (Lund)
TOBLOR Consulting —Lund
- Engelska
- Masterexamen
- Projektledning
Ansök direkt
11d
Country Manager Sweden
Eolus —Malmö
- Engelska
- Masterexamen
- Ledarskap
Data Management Specialist | Data & Product
Inter IKEA Group —Malmö
- Heltid
- Agile
- Företagsekonomi
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4d
Sr. Project Manager – R&D
Nipro —Malmö
- Kontor
- Masterexamen
- Projektledning
Control System Integrator
Nexer Telescope AB —Lund
- Heltid
- Engelska
- Masterexamen
- Kandidatexamen
9d
Valideringsingenjör (Life Science)
Capgemini Sweden —Malmö
Senior Research Scientist - Toxicology - Camurus (Lund)
TOBLOR Consulting AB —Lund
- Heltid
- Engelska
- Masterexamen
3d
Valideringsingenjör (Life Science)
Capgemini Sogeti —Malmö
Logistics Quality Manager
foodora —Malmö
- Heltid
- Kommunikationsfärdigheter
Atlassian Solution Architect
Pacera —Malmö
- Heltid
- Analytisk förmåga
- Agile
- Kommunikationsfärdigheter
12d

Jag vill få den senaste jobbevakningen för regulatory compliance i malmö

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Hands-on Regulatory Affairs Expert

Sunmedic AB
Vellinge

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Jobbinformation

Tillsvidare | Heltid

Kvalifikationer

Engelska
Masterexamen
Kandidatexamen
Övervakning
Organisationsförmåga

Fullständig jobbeskrivning

Sunmedic is a medical device company focused on developing safe and effective products. We are looking for a hands-on Regulatory Affairs Expert who can take ownership of technical documentation, ensure regulatory compliance, and work closely with quality and development teams.
What you will do

Prepare, maintain, and update technical files and regulatory documentation in line with EU MDR and other applicable regulations.
Handle regulatory submissions (EU MDR) and manage lifecycle activities including updates and variations.
Support and maintain the quality management system (ISO 13485), including quality control documentation and records.
Review and assess design changes, labeling updates, and material changes for regulatory impact.
Collaborate with Quality Assurance and R&D teams to ensure technical documentation is complete, accurate, and audit-ready.
Prepare for and support audits and inspections by notified bodies and competent authorities.
Contribute to post-market surveillance activities and the preparation of related reports (e.g., PMCF, PSUR).
Monitor regulatory updates and implement necessary changes in technical files and quality documentation.

Who you are

A practical and detail-oriented regulatory professional who enjoys working directly with technical files and documentation.
Comfortable working in a fast-paced environment where you need to deliver concrete regulatory outputs.
Proactive in identifying compliance gaps and implementing practical solutions.
Clear communicator who can work effectively with Quality, R&D, and external auditors.

What you have

Bachelor’s or Master’s degree in Life Sciences, Engineering, or a related field.
At least 2 years of ,hands-on regulatory affairs experience, in the medical device industry.
Solid experience preparing and maintaining, technical files, and working within a quality management system (ISO 13485).
Good knowledge of EU MDR requirements and regulatory submissions.
Strong organizational skills and attention to detail when managing documentation and multiple tasks.
Proficiency in English (written and spoken).

Nice to have:

Experience with post-market surveillance and clinical evaluation reports.
Familiarity with US FDA 510(k) or UK MDR submissions.
Previous involvement in audits or inspections.

What we offer

Competitive salary and benefits.
Flexible working arrangements.
The opportunity to work closely with product development and quality teams on real regulatory deliverables.

How to apply
Please send your CV and a short cover letter describing your experience with technical files, quality systems, and regulatory submissions, to [email protected]. Mention any specific documentation or projects you have worked on.

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Förfina din sökning

regulatory compliance jobb i malmö

Hands-on Regulatory Affairs Expert

Regulatory Affairs Associate

Sustainability Compliance & Reporting Intern

Junior Kvalitetskonsult (Life Science)

Compliance & Validation Specialist

Senior Regulatory Affairs Manager - Camurus (Lund)

Junior Kvalitetskonsult (Life Science)

Financial Controller

Senior Product Manager

Sr. Project Manager – R&D

Senior Regulatory Affairs Manager - Camurus (Lund)

Country Manager Sweden

Data Management Specialist | Data & Product

Sr. Project Manager – R&D

Control System Integrator

Valideringsingenjör (Life Science)

Senior Research Scientist - Toxicology - Camurus (Lund)

Valideringsingenjör (Life Science)

Logistics Quality Manager

Atlassian Solution Architect

Jag vill få den senaste jobbevakningen för regulatory compliance i malmö

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