Supplier Quality Manager

• Conducting supplier quality audits at Suppliers to ensure independently the compliance of HARTMANN
• Support the technical development of the suppliers and provide them with ad-hoc support
• Maintain all SQM-activities related to product and supply quality for assigned product portfolios and projects
• Applying the requirements of reliable regulations and standards (eg. ISO 9001, ISO 13485, MDR, FDA) at suppliers
• Supervision of the implementation of corrective measures
• Evaluating the effectiveness of implemented actions by supplier
• Communication across the entire global company with the relevant international stakeholders

• Technical university education
• Experience in conducting of external supplier audits in the medical device industry
• Qualification as lead auditor for ISO 9001, ideally ISO 13485
• Experience with working in the area of medical devices acc. MDR and FDA.
• Willingness and desire to work and communicate in an international environment across the company
• Willingness to travel internationally
• Business Proficiency English
• One or several of the following languages would be beneficial: German, French, Spanish, Turkish or Arabic
• Independence, diligence, precision
• Systematicity and technical thinking preferable production experience
• Willingness to learn new things
• Experience in the field of at least 5 years as auditor

• Interesting and responsible work in a prosperous company
• Working with in an international team and environment
• Working internationally
• Long-term stable work
• Possibility of individual development and education
• 25 days of vacation
• Benefit card
• Annual bonus after meeting the conditions
• Contribution to company catering
• Contribution to pension insurance

Hartmann