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R&D Material Compliance Specialist (m/w/x)
Technical ownership of material compliance for medical device materials and processes at a medical technology development center. Several years of experience in regulated industrial environments required. Up to 40% mobile work, 30 days annual leave.
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Anforderungen
- Bachelor's or Master's degree in Materials Science, Engineering, Chemistry, or related technical discipline
- Several years of experience in regulated industrial environment (medical devices, pharmaceuticals, life sciences, electronics, automotive, aerospace)
- Practical experience managing material compliance requirements throughout product development lifecycle
- Proactive mindset, ability to work independently and coordinate international stakeholders
- Genuine interest in environmental regulations and sustainable product development
- Experience in medical device industry (advantageous, not essential)
- Solid knowledge of global material compliance regulations (REACH, RoHS, PFAS, SCIP, TSCA, CLP, SVHC, CMR, Conflict Minerals)
- Good understanding of sustainable materials, hazardous substances, and environmental compliance
- Experience developing compliant processes, documentation, and data management systems
- Strong project management and stakeholder management skills
- Excellent analytical thinking and problem-solving abilities
- Clear communication skills, confidence to advise engineers, teams, and stakeholders
- Fluent written and spoken English
- Willingness to travel occasionally within Europe and internationally
Aufgaben
- Provide technical ownership of material compliance for medical device materials and processes
- Coordinate material compliance programs and data management across cross-functional teams
- Represent EMEA R&D in global and regional material compliance networks
- Conduct regulatory surveillance and interpret material compliance legislation and standards
- Assess regulatory impact and coordinate compliance data for product development
- Continuously improve material compliance systems, processes, and databases
- Support product design, development, and certification with material compliance
- Deliver training and provide subject matter expertise on material compliance
- Lead material compliance initiatives and manage stakeholders
- Engage with industry and contribute best practices in external working groups
- Provide internal consultancy and management advisory on material compliance and regulations
- Manage supplier and external partner relationships
- Comply with QMS, GDP, and GMP requirements
Berufserfahrung
Ausbildung
Sprachen
Tools & Technologien
Benefits
- Up to 40% mobile work
- Flexible work time model
- Overtime compensation
- 30 days of annual leave
- Holiday bonus
- Christmas bonus
- Corporate benefits discounts
- Company pension scheme
- Capital-forming benefits
- Subsidized company restaurant
- Employee Assistance Program
- Public transportation subsidy
- Free parking spaces
- Bike leasing
- Car leasing
- Company sports groups
- Inhouse company gym
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens Olympus Surgical Technologies Europe 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 Olympus Surgical Technologies EuropeÜber das Unternehmen
Das Unternehmen ist ein globales Medizintechnikunternehmen, das Lösungen für die Früherkennung, Diagnose und minimalinvasive Behandlung von Erkrankungen bereitstellt.
olympus-oste.euNejo bewertet ihn, und bringt ihn danach gemeinsam mit dir in Bestform.
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