Product Development Engineer (m/w/d) - 3D Druck und Materialwissenschaft

Date: Sep 18, 2026

Location: Bensheim, DE, 64625

Company: Dentsply Sirona, Inc

Requistion ID: 84209 

 

Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with over a century of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands.

 

Dentsply Sirona’s products provide innovative, high-quality, and effective solutions to advance patient care and deliver better and safer dental care. Dentsply Sirona’s headquarter is located in Charlotte, North Carolina. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.dentsplysirona.com for more information about Dentsply Sirona and its products.

 

Development Engineer/Scientist (m/f/d) with a Focus on Additive Manufacturing & Process Development for Dental Medical Devices

We are an innovative, internationally operating company in the field of dental medicine. For our product development team, we are looking for talented and motivated colleagues who want to shape the future together with us, whether you are an early-career professional or an experienced expert.

 

Your Responsibilities

 

Research & Development of Innovative Dental Applications

 

  • Development and implementation of innovative processes for dental 3D printing
  • Development, optimization, and verification of 3D printing processes for dental medical devices in collaboration with internal and external partners
  • Characterization and evaluation of material and process parameters to ensure product quality
  • Literature and patent research to support modern product concepts

 

Cross-Functional Collaboration

 

  • Working in international, cross-site teams comprising R&D, Engineering, Manufacturing, Regulatory Affairs, and Product Management/Marketing
  • Preparation of reports, presentations, and technical documentation in both German and English

 

Regulatory Affairs & Quality Standards

 

  • Planning, execution, and documentation of process verifications and technical investigations in compliance with applicable standards and regulatory requirements, particularly regarding biocompatibility and material properties
  • Preparation of technical dossiers for regulatory submissions (FDA, CE/MDR)
  • Ensuring compliance with all relevant standards and regulatory requirements

 

Project Management & Innovation

 

  • Independent leadership and management of development projects, including resource and timeline management
  • Structured problem-solving and continuous product improvement

 

Process & Quality Optimization

 

  • Optimization of product characteristics and manufacturing processes through Design of Experiments (DoE), experimental investigations, and data-driven analysis
  • Participation in risk analyses, validation activities, and quality control processes

 

What You Bring

 

  • 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
  • Enjoyment of hands-on laboratory work as well as the planning, execution, documentation, and evaluation of 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

 

Preferred Qualifications

 

  • Experience with verification and validation activities for medical devices, as well as the associated standards and regulations
  • Knowledge of material chemistry for 3D printing processes, particularly photopolymers, is desirable
  • Knowledge of regulatory requirements (e.g., MDR, 21 CFR 820, and FDA guidance documents) and dental product standards

 

 


Equal Opportunity Employer: Dentsply Sirona is an Equal Opportunity Employer. All qualified applicants will be considered without unlawful discrimination or regard for race, color, religion, sex, sexual orientation, sexual or gender identity, national or ethnic origin, age, marital status, disability, genetic factors, military and veteran status, or any other characteristics protected by applicable local law.

Eligibility: All successful applicants must be eligible to work in the country the position is based.

Assistance: If you need assistance with completing the online application due to a disability, please send an accommodation request to accommodationrequest@dentsplysirona.com.

Agencies: Please note that Dentsply Sirona does not accept or respond to unsolicited requests or applications submitted by Recruitment Agencies/ Search Firms.

Notice on Fraudulent Job Offers: Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information: careers.dentsplysirona.com.