Validation and Qualification Specialist (m/f/d)

Sei unter den ersten Bewerbenden.
Nur für registrierte Mitglieder
Geisingen
EUR 50.000 - 70.000
Sei unter den ersten Bewerbenden.
Vor 5 Tagen
Jobbeschreibung

Validation and Qualification Specialist (m/f/d)

Validation and Qualification Specialist (m/f/d)

06/23/2025

Your job in medical technology - at a global market leader, start-up and family business all in one.

PAJUNK is an owner-managed family business with around 700 employees worldwide and is headquartered in Geisingen, southern Germany. We develop needs-orientated medical products with the aim of enabling medical professionals worldwide to focus on what really matters: the patients.

We combine the strength of a market leader with the agility of a start-up. You will benefit from a secure job with innovative products in a crisis-proof industry and an international environment. In addition, you can expect short decision-making processes and respectful cooperation, so that real teamwork is possible.

Support our team at the earliest possible date as a Validation and Qualification Specialist (m/f/d).

  • You will take responsibility for the validation and qualification of our medical products, manufacturing processes and measurement systems.
  • By creating methodological content when compiling validation and qualification activities, you will contribute to maintaining the overall documentation.
  • With the help of risk assessments, such as FMEAs, you will identify critical process risks and derive targeted measures.
  • Together with our team, you will ensure that the regulatory requirements of our technical processes, systems and software are met.

You will also actively shape existing and new production processes for product development projects in collaboration with the specialist departments.

What you bring with you

  • Ideally a degree in engineering, natural sciences or comparable qualification
  • At least 2 years of professional experience in quality management or quality assurance, ideally in a medical technology environment
  • Experience in project management and knowledge of national and international regulatory requirements for medical devices
  • Motivation to independently understand complex issues and ability to present them in a structured manner

Good written and spoken English skills

You can look forward to

  • Varied tasks and the opportunity to help shape future-oriented projects holistically from the idea to implementation
  • A modern working environment and openness to new technologies
  • An attractive salary package (voluntary Christmas and holiday bonus, voluntary performance bonus, travel allowance depending on distance travelled)
  • Flexible working hours through flexitime accounts
  • Home office by arrangement
  • A comprehensive range of further training opportunities to promote your development
  • A comprehensive health and sports programme (Hansefit, ergonomic workstations, company sports, health days, company doctor, free vaccinations)
  • Seasonal and delicious food, freshly prepared by our kitchen team
  • Find out more about our numerous benefits here

Do you have any further questions?

Annalen Ohnmacht in the HR department will be happy to answer your questions by phone on +4977049291547.