QM-Expert (m/w/d)

Leipzig  ‐ Vor Ort

Schlagworte

Qualitätsmanagement Audits Iso 13485 Change Control Softwaredokumentation Produktlebensdauer Risikomanagement

Beschreibung

Senior Quality Engineer as Quality Management Expert (m/w/d)

Key Responsibilities:
  • Manage and improve the quality management system based on ISO 13485:2016
  • Plan, conduct and report internal and external audits
  • Prepare and take part in regulatory inspections
  • Ensure auditing and manufacturing documentation is kept up to date by the responsible departments
  • Manage periodic and ongoing review of standards, documents and procedures
  • Review the batch documentation of the medical devices
  • Problem-solving for ongoing process improvements
  • Manage Nonconformances and perform and document root cause investigations
  • Issue and manage Corrective and Preventive Actions (CAPAs)
  • Perform trainings on the quality management system
  • Coordinate the change control procedure within the company
  • Support management review
  • Keep the Technical Documentation up to date
  • Support validation including computer system validation and data integrity topics
  • Coordinate and serve as the contact with contract organizations and service providers related to quality aspects
  • Ensure effective Risk Management
  • Manage supplier qualification and evaluation
  • Responsible for complaint handling and post market surveillance


Requirements:
  • Completed bachelor or master's degree (preferred) in biomedical engineering or equivalent degree in technical/technological/bioscience field.
  • Minimum two years of experience in quality management in a medical device company
  • Demonstrated experience in quality oversight and management of products through the product lifecycle
  • Knowledge of the ISO 13485:2016 standard and EU MDR (Medical Device Regulation)
  • Internal auditor qualification
  • Ability to take over the function as quality management representative and deputy person responsible for regulatory complianceaccording article 15 MDR
  • Affinity to standard IT systems like MS office
  • Proficient in German and English, both written and spoken
  • Self-starter and team player


What we offer:
  • Permanent employment: With a working time account and overtime compensation, company pension plan, comprehensive insurance package, and generally a permanent contract.
  • Security through reliable payment: Attractive annual salary, punctual payment, full social security, continued payment of wages during vacation and illness.
  • A network of renowned companies: This provides you with a wide range of offers and quick access to exciting challenges.
  • Partnership: Individual support before, during, and after the completion of the client assignment.
  • Clear processes: These enable you to have direct and consistent communication with us.
  • Support for job start, career change, or re-entry: Through comprehensive advice, resume design, and personal expertise.


Perfect match?! Send your documents (resume, certificates, references) via the application link or by email to l.kramer[at]progressive.de.

If it's not suitable for you, reach out to your network - we would be thrilled about a recommendation!

A new opportunity, fresh impulses, and a perspective with a strong partner - Progressive®

Apply now!

Dieser Geschäftszweig der SThree GmbH betreut die ausgeschriebene Stelle im Auftrag ihres Kunden.
Start
08/2024
Dauer
12
Von
Progressive IT
Eingestellt
26.07.2024
Projekt-ID:
2778069
Vertragsart
Freiberuflich
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