PD Engineer (f/m/d)

freudenberg; Würselen; Vor Ort; EUR 42.000 - 62.000; Vollzeit

Zusammenfassung

Freudenberg Medical Hemoteq GmbH in Würselen, Germany, seeks an entry-level mechanical/biomedical engineer to help design and develop medical devices. You will work on specifications, prototypes, and documentation to ensure regulatory compliance and manufacturability.

You will participate in risk assessments, design reviews, and verification testing, collaborating with cross-functional teams to deliver safe, effective products on schedule.

Qualifikationen

• Bachelor's or university degree in Engineering (Mechanical, Biomedical, or related).
• 0–3 years engineering experience in medical devices or related field (internships ok).
• Familiarity with GMP and regulatory requirements for medical devices.
• Knowledge of 3D modeling and technical drawings.
• Basic prototype testing and manufacturability awareness.

Aufgaben

• Assist in design and development of medical devices with specs, prototypes, and design docs.
• Support risk assessments, design reviews, and verification testing for safety and efficacy.
• Assist build/testing of prototypes; select materials and develop test methods.
• Collaborate across NPI, manufacturing, quality, regulatory, suppliers, and customers.
• Maintain design documentation and coordinate testing with partners to meet timelines.
• Support product launches and resolve technical issues during transition to production.
• Contribute to early-stage innovation and feasibility studies under senior guidance.

Kenntnisse

GMP Knowledge

3D Modeling

Technical Drawing

Prototype Testing

Communication

Ausbildung

Bachelor's degree in Engineering

Jobbeschreibung

Working at Freudenberg: We will wow your world!

Responsibilities:

• Assist in the design and development of new and existing medical devices by developing specifications, prototypes, and design documentation in compliance with regulatory and quality requirements.
• Support the preparation of design/development documentation; participate in risk assessments, design/project reviews, and verification testing to ensure product safety and efficacy.
• Assist in the build and testing of prototype devices, select appropriate materials, and assist with developing processes, test methods and characterization studies.
• Collaborate cross-functionally with NPI, manufacturing, quality, regulatory, suppliers and customers to learn and support design/process activities that ensure manufacturability, regulatory compliance, and cost-effectiveness.
• Assist in the preparation and maintenance of design/development documentation, in accordance with ISO, applicable regulatory and company standards.
• Participate in project execution by managing tasks, participating in team meetings, maintaining accurate engineering documentation, and coordinating testing activities with internal and external partners to meet project timelines and deliverables.
• Support product launches by providing engineering input during transition to NPI/ production, resolving technical issues, and contributing to continuous improvement efforts.
• Contribute to early-stage innovation efforts by researching new technologies and supporting technical feasibility assessments under the guidance of senior engineers.
• Ability to manage multiple tasks and adapt to a changing, fast-paced environment.

Qualifications:

• Bachelor's/University degree in Engineering (Mechanical, Biomedical, etc.), or related science/technical field.
• 0-3 years of engineering in medical device or related industry experience (or Internship or academic experience).
• Familiarity with GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements.
• Working knowledge or coursework in 3D solid modeling and technical drawings
• Basic understanding of creating prototypes using various materials and techniques to test and validate product designs.
• Awareness of Design for Manufacturability (DFM) principles to design products that are manufacturable and cost effective.
• Ability to communicate technical ideas clearly, ask thoughtful questions, and document work accurately.

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical Hemoteq GmbH