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Product Development Engineer – 3D Druck, Materialwissenschaft
Dentsply Sirona. Research and develop innovative dental applications .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing and optimizing 3D printing processes for dental medical devices, ensuring compliance with regulatory standards such as FDA and MDR. Proficient in material characterization and verification activities, with strong analytical and problem-solving skills in interdisciplinary environments.
Highest-signal resume keywords
3D Printing Process DevelopmentMaterial CharacterizationRegulatory Compliance (FDA, MDR)Verification and Validation ActivitiesProject Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Additive ManufacturingProcess DevelopmentExperimental DesignData-Driven AnalysisTechnical DocumentationMaterial ChemistryQuality ControlRisk AnalysisTechnical Dossier PreparationLaboratory Work
Soft Skills
TeamworkCommunicationAnalytical ThinkingStructured Problem-SolvingSelf-Driven Work Ethic
Industry Keywords
Medical Device IndustryDental ApplicationsRegulated Technical EnvironmentMDR Standards21 CFR 820FDA Guidance DocumentsPhotopolymersInterdisciplinary CollaborationProcess VerificationProduct Development
About the role
Key responsibilities & impact- Research and develop innovative dental applications
- Develop and implement innovative processes for dental 3D printing
- Develop, optimize, and verify 3D printing processes for dental medical devices with internal and external partners
- Characterize and evaluate material and process parameters to ensure product quality
- Conduct literature and patent research to support modern product concepts
- Work in international, cross-site teams across R&D, Engineering, Manufacturing, Regulatory Affairs, and Product Management/Marketing
- Prepare reports, presentations, and technical documentation in German and English
- Plan, execute, and document process verifications and technical investigations in compliance with standards and regulatory requirements
- Prepare technical dossiers for FDA and CE/MDR regulatory submissions
- Ensure compliance with relevant standards and regulatory requirements
- Independently lead and manage development projects, including resources and timelines
- Apply structured problem-solving and continuous product improvement
- Optimize product characteristics and manufacturing processes using Design of Experiments, experimental investigations, and data-driven analysis
- Participate in risk analyses, validation activities, and quality control processes
Requirements
What you’ll need- Successfully completed university degree in a scientific or technical discipline (e.g., Engineering, Materials Science, Medical Engineering, Chemistry, Physics, or Process Engineering)
- Several years of professional experience in product development, ideally within the medical device industry or a comparable regulated technical environment
- Interest in, and ideally initial experience with, additive manufacturing, material characterization, or process development
- Hands-on laboratory work experience and ability to plan, execute, document, and evaluate experimental studies
- Passion for technology, analytical thinking, and innovation
- Willingness to quickly familiarize yourself with new topics and work in interdisciplinary environments
- Strong teamwork and communication skills, combined with a structured and self-driven way of working
- Excellent German and English language skills, both written and spoken
- Experience with verification and validation activities for medical devices, as well as associated standards and regulations
- Knowledge of material chemistry for 3D printing processes, particularly photopolymers, desirable
- Knowledge of regulatory requirements, including MDR, 21 CFR 820, FDA guidance documents, and dental product standards
Benefits
Comp & perks- Equal Opportunity Employer commitment
- Disability accommodation assistance during the application process