Quality Management Engineer (m/f/d)

SCHÖLLY FIBEROPTIC GMBH; Denzlingen; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading company in medical technology is seeking a Quality Management Engineer to oversee validation management processes. The ideal candidate will have a strong background in quality management, extensive experience in the pharmaceutical or medical technology fields, and fluency in German (C2) and English (C1). We offer a flexible working environment, performance-related remuneration, and opportunities for professional development.

Leistungen

Flexible working hours

Performance-related remuneration

Attractively subsidized pension scheme

Hansefit membership

Leaserad options

Qualifikationen

• Several years of professional experience in qualification and validation.
• Experience in a pharmaceutical or medical technology environment.
• Good knowledge of German and English.

Aufgaben

• Create specifications for validation management.
• Ensure testing and release of validation activities.
• Conduct internal audits and participate in inspections.
• Manage CAPA processes and documentation.

Kenntnisse

Validation management

Quality management

German (C2)

English (C1)

Strong communication skills

Ausbildung

Technical or economic studies

Jobbeschreibung

You Are Here

• Schoelly
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SCHÖLLY has been developing endoscopic visualization systems that are used for the benefit of people for 50 years.

Customer-focused, cooperative, imaginative, humane, competent and value-creating - these are the values that define us and that give our teams room to grow and thrive.

Join us and lead your own success story with us.

Your Contact

Andrea Hauschel

Senior Human Resources Specialist

[phone]

working(at)schoelly.de

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Quality Management Engineer (m/f/d)

Your responsibilities

• Creation of specifications for validation management (qualification, processes, computer systems, test methods) and its continuous development
• Ensuring, testing and releasing validation activities and documents in development and production
• Training in methodological skills and guiding employees in the implementation of validation management
• Conducting internal audits and participating in inspections and audits as a subject matter expert
• Participation in CAPA management - initiation, processing and monitoring of correction and improvement measures using QM methods
  
  

Your profile

• Completed technical or economic studies, ideally with relevant additional qualifications in the area of quality management
• Several years of professional experience in the area of qualification and validation, ideally in a pharmaceutical or medical technology environment (Good Manufacturing Practice / GMP)
• Very good knowledge of German (GER C2) and English (GER C1)
• A confident demeanor, strong communication skills and a special awareness of quality and care in documentation complete your profile
  
  

What we offer

• Opportunities for development in a flexible company with a strong group in the background
• Motivated colleagues, flat hierarchies, short decision-making processes and a spirit of partnership
• Performance-related remuneration, flexible working hours with home office options, an attractively subsidized pension scheme and favorable special conditions for a wide range of private insurance policies
• Hansefit and Leaserad
  
  

We look forward to receiving your online application stating your salary expectations and the starting date.

Apply Now