Job requirements and application form

R&D Engineer
(923076)

Job description

The opportunity: As an R&D Engineer, you will play a key role in the development of innovative medical devices for minimally invasive surgical and radiation oncology procedures. Working as part of a multidisciplinary R&D team, you will contribute to all stages of the product development lifecycle, from concept evaluation and design verification to validation and regulatory documentation. This is an exciting opportunity to combine hands-on engineering, technical problem-solving, and cross-functional collaboration while helping bring cutting-edge technologies to patients worldwide. In this position you will be asked to: • Contribute to the development of innovative medical devices throughout the entire product development lifecycle. • Design, execute, and document verification and validation activities to ensure product performance and quality. • Develop engineering solutions, evaluate design alternatives, and support technical risk management. • Collaborate with cross-functional teams, suppliers, manufacturers, and external development partners. • Prepare technical documentation in compliance with FDA Design Controls and support regulatory submissions. • Contribute to continuous product improvement, innovation, and intellectual property activities.

Job requirements

• Bachelor’s degree in biomedical engineering, Materials Science, or a related Engineering discipline. • 2-5 years of experience in medical device R&D (or an M.Sc. with relevant experience). • Experience with medical device product development, preferably within a stage-gate development process. • Working knowledge of FDA Design Controls is required; familiarity with ISO 14971, ISO 10993, IEC 60601, or other relevant medical device standards is an advantage. • Experience with design verification and validation, technical documentation, and product development deliverables. • Experience with implantable or bioabsorbable medical devices and familiarity with medical device manufacturing processes are considered an advantage. • Experience in statistics is required. Working knowledge of statistical analysis software (e.g., Minitab) is a plus. • Proficiency in Microsoft Office applications is required. • Working knowledge of SolidWorks is an advantage. • Strong analytical and problem-solving skills, with the ability to make sound technical decisions. • Excellent verbal and written communication skills, with the ability to collaborate across cross-functional teams and present technical information to stakeholders. Location: Netanya

Submit application

*First name:
*Last name:
*Phone:
*Email:
*City:
 
*CV:
Drag a file here to uploadorSelect file
Further remarks:
*Do you hold a B.Sc. or higher in Biomedical, Materials, Chemical Eng?
*Do you have 3+ years of R&D experience in the medical device industry?
*Do you have experience in Biocompatibility & Chemical Characterization / E&L?
*Have you led or supported Packaging Validation for devices?
*Are you available for a full-time, 100% on-site role in Netanya?
*
privacy policy

Share this job opportunity with friends:

promo image