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
You will work alongside in IT department collaborate with other teams in the DGS Poland factory, Project Managers, Subject Matters Expert from Manufacturing, Logistics, Technical Department, Quality. Our goal is to develop and optimize the holding's operational activities by providing IT support and solutions.
- Possibility to work with Validations, Risk assessments and systems documentation amongst other tasks;
- Full-time work agreement in the international developing organization;
- Possibility to learn (courses offered) and improve English in our international environment;
- Great opportunities for usage of newest technology;
- Social benefits (private medical health care, insurance, sport card, discount card etc.).
- Drive compliance assessments.
- Drive the assigned validation activities in collaboration with Manufacturing and Quality Management System validations.
- Support the internal validations.
- Review and approve validation protocols, deviations and reports.
- Approval of Risk Documentation (e.g. FMEA) and Process Validation Master Plans.
- Review of procedures, work instructions, standard maintenance documents or master documents.
- Prepare and review production systems documentation.
- You have previous experience in Computer Validation, GxP Risk assessment and Validations in the medical device/pharma industry and are familiar with ISO13485:2016, 21CFR820, MDSAP.
- You have an excellent communication skills and pro-active attitude.
- You have a good problem-solving skills and ability to manage priorities.
- Manufacturing business experience will be an advantage.