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Job Post Details

Quality Engineer for Medical Device Development (m/f/d) - job post

Gerresheimer
3.1 étoile(s) sur 5
4600 Olten, SO
100%, Temps de travail : 90-100%

Détails de l'emploi

Correspondance entre ce poste et votre profil.

Type de poste

  • 100%
  • Temps de travail : 90-100%

Lieu

4600 Olten, SO

Description du poste

Company Description


We are on an exciting journey as we take an active role in creating the future of the digital healthcare ecosystem. You will be supporting a highly motivated and dynamic management team on its mission to build new business opportunities accross the Gerresheimer Group.

As a listed company in the MDAX, Gerresheimer is a leading global partner to the healthcare and cosmetics industry. We generate sales of over 1.9 billion euros and have around 11,000 employees worldwide.

www.gerresheimer.com


Job Description


Role

  • Interest in the development of complex (electronic, software and mechanic) medical devices
  • Defining and ensuring compliance with quality requirements for drug delivery systems and medical devices in development projects
  • Ensuring the conformity of our products and product documentation over the entire product life cycle – focus on development and industrialization – Design Control
  • Collaboration in risk analyses
  • Creation / approval of documents for design verification / design validation
  • Creation / Release of Test Plans / Test Setups / Design of Experiment
  • Review and approve changes to product design and manufacturing processes
  • Contact person for customers and suppliers regarding product quality (incl. measures such as NC, CAPA, SCAR, etc.)
  • Collaboration in the equipment qualification / process validation and evaluation of external production partners
  • Contact person for quality-related questions in the context of audits by customers or authorities

Qualifications


Profile

  • Completed technical or scientific education or equivalent
  • Several years of experience in working in the field of medical technology products, pharmaceuticals and/or in-vitro diagnostics
  • Practical experience in the risk management method for medical devices
  • Practical experience in the application of quality and problem-solving techniques
  • Knowledge in the interpretation and implementation of regulatory requirements for medical devices (MDR, EN ISO 14971, 21 CFR 820, EN 13485)
  • Structured and result-oriented way of working
  • Willingness to proactively participate and make things happen, ability to prioritize and make decisions
  • Solution-oriented and communicative personality
  • Confident in communication across all hierarchical levels, internally and with customers
  • Willingness to travel (approx. 10%)
  • Very good oral and written language skills in German (B2) and English (C1)

Additional Information

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