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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 13485, 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. Have we aroused your interest? Then we look forward to receiving your complete online application with CV, letter of motivation, references and diplomas.
For further information, please contact Mr. Richard Büchi, Director Human Resources ,
If you have any technical questions, please contact Ms. Anna Kohler, CO-Director Quality Management & Regulatory Affairs, tel. +41 32 332 70 73.
Seniority level Seniority level Associate
Employment type Employment type Full-time
Job function Job function Quality Assurance
Industries Medical Equipment Manufacturing
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