Imagine going to work every day knowing that you are improving the quality of life for many people by manufacturing high-quality medical products. You have the opportunity to become part of this mission.
Nipro PharmaPackaging Germany GmbH, based in Münnerstadt, is part of Nipro Corporation Japan, a globally leading healthcare company. At our Münnerstadt site, we operate two plants with around 490 employees, producing high-quality glass syringes and glass vials for the pharmaceutical industry. We combine a long company history with state-of-the-art manufacturing technologies.
We are currently looking for a
Your Responsibilities – with a strong focus on customer partnership and continuous improvement
In this role, you take ownership of customer‑related quality management topics and actively shape a modern, process‑oriented Quality Management System in a highly regulated environment.
- Ensure, develop and continuously improve the Quality Management System in compliance with ISO 9001, ISO 15378 and ideally ISO 13485
- Define, implement and monitor quality objectives and KPIs to drive sustainable improvement of products and processes
- Act as a trusted quality interface for selected customers, representing the company professionally in customer meetings and audits
- Manage customer feedback and quality issues with a strong focus on root cause analysis, transparent communication and effective CAPA implementation
- Prepare clear, structured quality reports and analyze quality data to improve products, processes and long‑term customer relationships
- Independently prepare, negotiate and maintain Quality Assurance Agreements (QAAs) in close collaboration with customers
- Contribute to regulatory and quality‑related projects in the medical device environment, e.g. in the context of importer or distributor activities
What We Offer – your perspective with us
- A responsible and varied role with real influence on the design and development of quality management processes
- Close cooperation with management and cross‑functional teams, supported by short decision‑making paths
- A challenging, highly regulated environment with a strong focus on customer satisfaction and quality excellence
- A collegial, open working culture with teamwork, professional exchange and opportunities for personal development
Your Profile
- Completed technical or scientific education or a comparable qualification
- At least 3 years of experience in Quality Assurance or Quality Management, preferably in a regulated industry
- Very good knowledge of ISO 13485 and ISO 9001; experience with ISO 15378 is a strong advantage
- Hands‑on experience with common quality methods and tools (e.g. 8D, FMEA, Ishikawa)
- Confident handling of quality documentation, audits and regulatory requirements
- Very good German and English skills, written and spoken
- A structured, self‑reliant and solution‑oriented working style with strong communication skills and customer focus
Severely disabled applicants and those with equivalent status will be given preferential consideration in case of equal qualification.