DGS Business Services Sp. z o.o.

Regulatory Affairs Specialist

DGS Business Services Sp. z o.o.O firmie

DGS Business Services Sp. z o.o.

Oxygen

Szczecin

Regulatory Affairs Specialist

DGS operates in Poland since 2007. The company, initially under the name Oticon Polska Production, manufactured hearing aids at a manufacturing facility in Mierzyn. Over the course of its 10-year existence, the company expanded their production range to technologically advanced hearing aids and diagnostic equipment, as well as IT, HR, software development, quality assurance, finances and logistic services. Due to the dynamic growth and experienced staff, a decision was made in 2015 to create a new organisation, which would provide its services to companies being parts of the William Demant Group. Currently, DGS employs 2200 people in Poland and is constantly expanding its operations, while continuously hiring new employees.

Stable employment, ideal working conditions for professional development and a friendly atmosphere.

That's the foundation. But that's not all - we can offer much more.

Private health care

Summer cottages in Denmark

Free transportation

Cinema tickets

Company event

Car and bike parking

Company canteen

Sport club and gym membership

Working with us gives you the opportunity not only to plan your own work and be largely self-managed, but also to become a part of an experienced team of specialists capable of working in a dynamic and challenging international organization.

 
What is more:
  • full-time work agreement in the international developing organization;
  • possibility to learn (courses offered) and improve English in daily basis;
  • flexible working hours;
  • business trips;
  • social benefits (private medical health care, insurance, sport card, discount card, cinema tickets etc.).
What will your tasks be?
  • maintaining technical documentation for the Medical devices including documentation for private label products.
  • updating and reviewing regulatory documentation e.g. marketing materials.
  • participation in Regulatory projects.
  • attendance in design review of the design changes ECR. Performing  risk evaluation of the design changes. Handling of ECO, updating documentation relating to ECO.
  • supporting the other teams (RAP, RACA, RAFR) with creation and review of project deliverables.
If You have:
  • experience with Regulatory Affairs or you work in the medical devices business or any other well-regulated areas (e.g. pharmacology) for at least a year will be an advantage;
  • bachelor degree in medicine, chemistry, pharmacy or similar but your educational background is not decisive;
  • experience of working with MS Office, Database Systems and documentation systems;
  • good English skills enabling everyday communication;
  • analytical and communication skills;
  • ability to travel to Denmark at least six time per year;
  • systematic approach to your work, willing to get things to be done;
  • self-driven approach but the same time you are a strong team player who can develop and maintain good relations with stakeholders – so we are looking for your application!

Find out more - click on "Apply now"


Please write a cover letter and CV, adding the clause: in accordance with the Law of Personal Data Protection of 29.08.1997 (Journal of Laws No. 101, item 926) I give my consent to processing of my personal data contained in the offer for the recruitment process in DGS Poland Sp. z o.o. and DGS Business Services Sp. z o.o.

We do not return the applications. We will contact selected candidates.

DGS operates in Poland since 2007. The company, initially under the name Oticon Polska Production, manufactured hearing aids at a manufacturing facility in Mierzyn. Over the course of its 10-year existence, the company expanded their production range to technologically advanced hearing aids and diagnostic equipment, as well as IT, HR, software development, quality assurance, finances and logistic services. Due to the dynamic growth and experienced staff, a decision was made in 2015 to create a new organisation, which would provide its services to companies being parts of the William Demant Group. Currently, DGS employs 2200 people in Poland and is constantly expanding its operations, while continuously hiring new employees.

Regulatory Affairs Specialist

Working with us gives you the opportunity not only to plan your own work and be largely self-managed, but also to become a part of an experienced team of specialists capable of working in a dynamic and challenging international organization.

 
What is more:
  • full-time work agreement in the international developing organization;
  • possibility to learn (courses offered) and improve English in daily basis;
  • flexible working hours;
  • business trips;
  • social benefits (private medical health care, insurance, sport card, discount card, cinema tickets etc.).
What will your tasks be?
  • maintaining technical documentation for the Medical devices including documentation for private label products.
  • updating and reviewing regulatory documentation e.g. marketing materials.
  • participation in Regulatory projects.
  • attendance in design review of the design changes ECR. Performing  risk evaluation of the design changes. Handling of ECO, updating documentation relating to ECO.
  • supporting the other teams (RAP, RACA, RAFR) with creation and review of project deliverables.
If You have:
  • experience with Regulatory Affairs or you work in the medical devices business or any other well-regulated areas (e.g. pharmacology) for at least a year will be an advantage;
  • bachelor degree in medicine, chemistry, pharmacy or similar but your educational background is not decisive;
  • experience of working with MS Office, Database Systems and documentation systems;
  • good English skills enabling everyday communication;
  • analytical and communication skills;
  • ability to travel to Denmark at least six time per year;
  • systematic approach to your work, willing to get things to be done;
  • self-driven approach but the same time you are a strong team player who can develop and maintain good relations with stakeholders – so we are looking for your application!

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