Quality Manager (f / m / d)

Ziemer Ophthalmic Systems AG; Port; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

Join Ziemer Ophthalmic Systems AG as a Quality Manager, responsible for the QMS development and compliance. With your extensive experience in quality management and auditing, you'll ensure adherence to regulatory standards, enhancing our commitment to innovation in medical technology.

Qualifikationen

• At least 5 years' experience in quality management and conducting audits.
• Further training in quality management (SAQ, NDS, TüV or similar) is desired.
• Enjoy working in a small team with various stakeholders.

Aufgaben

• Carrying out internal and supplier audits in accordance with MDSAP.
• Implementing regulatory measures within the Quality Management System.
• Training and advising employees on quality management and regulatory issues.

Kenntnisse

Quality Management

Auditing

Regulatory Compliance

MS-Office

German

English

Ausbildung

Technical or commercial education

Technical university degree

Jobbeschreibung

We aim to enhance the lives of millions. Driven by our passion for innovation, we tirelessly develop cutting-edge products and services in ophthalmology. Become a part of the Ziemer Group's 25-year legacy and contribute to our ever-expanding team.

In this responsible position with place of work in Port & Brügg near Biel, you will be responsible for the maintenance and further development of the Quality Management System (QMS). As part of the QMS, you will ensure the implementation of regulatory requirements in collaboration with all parties involved.

Tasks

• Carrying out internal audits and supplier audits in accordance with MDSAP
• Controlling of "success-critical" suppliers
• Responsibility for and active involvement in the implementation of regulatory measures within the QMS
• Coordinating the implementation of measures to eliminate deviations / non-conformities
• Checking and creating various QMS documents
• Training and advising employees on quality management and regulatory issues
• Reviewing and approving validation documentation
• Supporting the evaluation and introduction of software in the QMS area
• Working on various projects

Profile

• Basic technical or commercial education with a flair for business administration and technology
• Technical) university degree an advantage, but not a requirement
• At least 5 years' experience in quality management and conducting audits (ISO 1348, MDSAP, MDR)
• Further training in quality management (SAQ, NDS, TüV or similar)
• Knowledge of medical technology or the pharmaceutical industry an advantage
• Quick comprehension, precise and solution-oriented way of working
• High quality awareness, enforcement power, flexibility
• Enjoy working in a small team and with various stakeholders
• Sound knowledge of MS-Office
• Very good knowledge of German and English

We offer you an exciting challenge in the growth-oriented medical technology market. As a committed and proactive personality, you can play a formative role in the future of our dynamic company.