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Responsibilities Act as Quality Assurance (design assurance) representative in development projects for platforms and product variants, as well as in Life Cycle Management activities.
Ensure compliant documentation in the projects and processes according to applicable standards, regulations, and customer requirements.
Drive the resolution of quality issues through effective collaboration across all organizational levels and functions.
Collaborate in projects and sub-projects for optimisation, harmonization, and further development of processes.
Monitor and analyze quality performance indicators and ensure transparent reporting to relevant stakeholders.
Perform investigations, prepare quality reports, and apply statistical methods to support data-driven decision-making.
Support quality-related communication with customers and actively participate in internal, customer, and regulatory audits.
Your profile Technical background, ideally in mechanical engineering, polymer engineering, or automation, combined with a degree in the natural sciences (FH, ETH, or university) or equivalent relevant professional experience.
Minimum two years of experience in a comparable role in the MedTech sector or comparable industry.
Strong analytical and methodological skills, with a structured and goal-oriented approach to problem-solving.
Ensuring compliance with applicable standards and regulatory requirements (e.g., ISO 13485:2016).
Proficiency in ERP systems (e.g., SAP), with familiarity in tools such as TrackWise, JIRA, Power BI, SAP Analytics Cloud, or AI-driven applications.
Good communication and language skills in writing and orally (German and English B2 or higher).
Additional Details Seniority level: Entry level
Employment type: Full-time
Job function: Quality Assurance
Industry: Medical Equipment Manufacturing
This job is active and accepting applications.
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