Polish Register of Ships looking for medical device specialists

The Polish Register of Ships (S.A.) extends a team of specialists responsible for certification of medical devices. The institution shall recruit auditors of quality management systems complying with ISO 13485:2016, including lead auditors, and industry experts supporting the conformity assessment process.
In the article
PRS develops competence in the field of medical devices
The Polish Register of Ships has been operating as a certification body in the medical sector for years, which is why the increasing number of proceedings and the changing EU regulations create a demand for new specialists. They are both wanted experienced auditors and technical experts involved in the design, manufacture or use of medical devices.
Cooperation may be implemented on the basis of a work contract or in a B2B model, which allows to adapt the scope and dimension of engagement to candidates' capabilities.
Scope of tasks for new specialists
The main responsibilities of PRS co-operators will include:
- participation in audits of quality management systems with manufacturers of medical devices complying with the requirements of ISO 13485:2016,
- independent audit – for candidates with appropriate qualifications,
- the development of audit reports,
- cooperation with a team of experts to assess the conformity of medical devices under the applicable MDR and IVDR regulations.
PRS requirements for candidates
People with technical, engineering, medical, pharmaceutical, biological, veterinary or other related education are invited to cooperate, who want to use their expertise in projects in the medical devices sector.
The PRS directs the offer to candidates with audit experience, as well as to technical experts with practical knowledge of medical devices – from the design and manufacture stage, through quality control to their use.
What PRS offers
Cooperation with the Polish Register of Ships S.A. is an opportunity to participate in the creation of a new area of activity of the certification body, work in a professional environment based on principles of impartiality and high quality standards and real impact on the development of the competence of the organization.
PRS S.A. offers attractive conditions for remuneration, flexible forms of cooperation, as well as the possibility of development through industry training, workshops and cooperation with a team of experts.
How to apply?
Please send your CV to:
anna.chruscikowska@prs.pl
with a note on the subject: "ISO 13485 Auditor".









