Audit Planning: Developing audit schedules and preparing for audits in line with relevant standards and regulations.
Conducting Client Audits: Verifying compliance of processes and documentation with quality and regulatory requirements.
Post-Audit Documentation: Preparing reports that include audit findings, recommendations, and necessary corrective actions.
Professional Development: Participating in training and courses to keep knowledge and competencies up to date.
Maintaining Client Relationships: Building positive relationships and providing guidance on medical device compliance.
Co-Developing New Services: Contributing to the development of new certification services and participating in the company’s development projects.
Requirements
Higher education in Electronics, Electrical Engineering, Automation, Medical Engineering, Biomechanics, or related fields.
Minimum of 3 years of professional experience in the area of medical devices.
Strong command of English - C1 .
Excellent communication skills, with an ability to build relationships easily.
Willingness to travel frequently, including internationally.
Familiarity with quality management systems for medical devices, including knowledge of regulations such as MDD, MDR, IVDD, IVDR, and EN ISO 13485 is a plus.
Our Client Offers
Work at one of our offices, with "home office" options available in other locations.
Opportunities to utilize and further develop your professional qualifications.
Collaboration with specialists in a friendly and cooperative atmosphere, including international work environments.
A mobile role with travel opportunities, including international trips.
A company car available for private use.
Flexible working hours (start between 7:00 and 9:30 a.m.).
Benefits package - private healthcare, co-funding for sports packages, accident insurance (NNW), and the option to join group insurance.
Additional social benefits, including subsidies for vacations and tickets to cultural events.
