Compliance Specialist

When you become part of the Demant familyyou also become part of our quest to make a life-changing difference for over 500 million people all over the world who suffer from hearing loss. Working with us you will be part of a world-leading hearing healthcare group that develops manufactures and sells highly advanced market-leading hearing solutions diagnostic equipment and personal communication.

• Help ensure compliance and quality in a global MedTech organization operating in a highly regulated environment
• Work with international teams on medical device and information security compliance
• Develop your expertise in ISO standards audits validation and risk management while working alongside experienced specialists
• Working in an international environment with Scandinavian work culture that promotes openness trust and diversity

We are waiting to hear from you!

We are looking for a Compliance Specialistto join our IT Compliance Team in Szczecin.
Our team supports more than 500 IT colleagues globally helping ensure that our products systems and processes meet medical device and information security compliance requirements. This is a great opportunity for someone who enjoys combining analytical thinking structured processes and stakeholder collaboration. You will work with colleagues across IT R&D Manufacturing Logistics Marketing and Sales while supporting compliance initiatives that directly contribute to delivering safe high-quality medical solutions.

You dont need to be an expert in every compliance area from day one-we are looking for someone eager to learn contribute and grow with the team.

• Full-time work agreement in an international organization
• Learning and development opportunities adapted to your needs and supporting your growth
• Hybrid work model combining remote work opportunities with work in an office in the Szczecin City Center
• Flexible working hours
• Benefits package including social benefits (private medical health care insurance sport card etc.)
• Scandinavian culture informal focused on equality independence open dialog and work-life balance

• Participate in internal compliance audits including ISO 13485 ISO 27001 and other quality standards

• Support validation activities by reviewing validation documentation reports and deviations
• Collaborate with project teams to ensure compliance requirements are incorporated into new systems and processes
• Help design and improve automated compliance workflows within IT systems
• Monitor compliance activities and follow up on corrective and preventive actions
• Support colleagues across the organization with compliance-related questions and best practices
• Update and develop internal procedures documentation and training materials
• Contribute to continuous improvement initiatives and help shape Demants future compliance strategy

• Hold a Bachelors degree in Engineering Computer Science Life Sciences Quality Management or a related field
• Have experience in quality assurance compliance validation testing risk management or regulated environments
• Have strong analytical skills and enjoy working with structured processes and documentation
• Pay close attention to detail and take ownership of your work
• Feel comfortable collaborating with international stakeholders
• Communicate confidently in English both spoken and written
• Are motivated to learn and develop within medical device and information security compliance

• Knowledge of ISO 13485 ISO 27001 SOC2 GMP 21 CFR Part 820 IVDR or similar regulatory frameworks
• Experience with internal audits validation or change control
• Familiarity with risk management methodologies
• Certifications such asISO 27001 Lead Auditor ISTQB ITIL or similar

Apply today!

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