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Product Lifecycle Manager – Medical Devices(m/w/x)
Managing product and design changes for tracheostomy devices, including DHF and regulatory documentation. 3+ years in medical devices and regulated environments required. Structured onboarding, welcoming culture.
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Anforderungen
- Bachelor’s degree in technical or scientific field
- At least 3 years experience in medical device or life-science industry
- Managing complex, cross-functional projects
- Practical experience in regulated environment (EN ISO 13485, EU-MDR, 21 CFR 820, MDSAP, ISO 14971, IEC 62366)
- Experience working within quality management system
- Confident use of MS Office 365
- Strong quality mindset
- Pragmatic implementation of technical, regulatory, documentation requirements
- Experience in international environment
- Analytical, structured, solution-oriented working style
- High initiative, sense of responsibility, reliability
- Holistic thinking and openness to new perspectives
- Bachelor’s degree in technical or scientific field
- At least 3 years experience in medical device or life-science industry
- Managing complex, cross-functional projects
- Practical experience in regulated environment (EN ISO 13485, EU-MDR, 21 CFR 820, MDSAP, ISO 14971, IEC 62366)
- Experience working within quality management system
- Confident use of MS Office 365
- Strong quality mindset
- Pragmatic implementation of technical, regulatory, documentation requirements
- Experience in international environment
- Analytical, structured, solution-oriented working style
- High initiative, sense of responsibility, reliability
- Holistic thinking and openness to new perspectives
Aufgaben
- Manage product and design changes throughout the lifecycle
- Manage project aspects of changes
- Create regulatory-compliant documentation (EN ISO 13485, EU-MDR, 21 CFR 820, MDSAP)
- Maintain and develop Design History Files (DHF)
- Maintain and develop technical documentation for medical devices (classes Is/m to IIa/b)
- Ensure complete traceability from user needs to design inputs/outputs, verification, validation, and risk management
- Act as technical point of contact for Design Control & Lifecycle Management
- Contribute to quality-related activities including risk management (EN ISO 14971), CAPAs, complaints, non-conformances, and post-market topics
- Plan and support transfer of new developments and product changes into production
- Participate in design reviews as an independent reviewer focusing on lifecycle and compliance
- Support audits and inspections
- Actively contribute to continuous improvement of lifecycle management processes
Berufserfahrung
Ausbildung
Sprachen
Tools & Technologien
Benefits
- Secure and responsible position
- Welcoming culture
- Friendly working atmosphere
- Colleagues at eye level
- Structured onboarding
- Professional and personal development support
- Idea management
- Room to shape processes
- Independent work
- Internal and external training opportunities
- Flexible working time models
- Flexitime
- Mobile working option
- Company events
- Free parking
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens Coloplast A/S erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Zur Originalanzeige bei Coloplast A/SÜber das Unternehmen
Das Unternehmen entwickelt und vermarktet Produkte und Dienstleistungen, die das Leben von Menschen mit persönlichen medizinischen Bedürfnissen vereinfachen.
Nejo bewertet ihn, und bringt ihn danach gemeinsam mit dir in Bestform.
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