Quality Assurance Lead

HumanTouch Surgical (continuing Human Xtensions) is a cutting-edge start-up developing multidisciplinary products in Minimally Invasive Surgery.

We seek a Quality Assurance lead to join our Quality and Regulatory Assurance team. The Quality Assurance lead will play a critical role in establishing and maintaining the design control activities and act as the focal point for quality assurance within the R&D department. You will also be responsible for regulatory support and customer complaint handling and partner with R&D, Operations, and other departments to continuously improve products and processes that meet all internal and external requirements and regulations.

Our offices are in Netanya. We offer a dynamic, innovative environment where you can make a significant impact while working alongside sharp, professional individuals passionate about the future of medical technology. If you’re ready for a new challenge and eager to grow, we’d love to hear from you!

Responsibilities

• Develop and execute quality design (design control) and quality assurance strategy for new product development and sustaining business activities.
• Lead all R&D projects from the design QA side through the design phases.
• Ensuring compliance with DHR and DMR requirements
• Developing and managing risk mitigation strategies for the project together with R&D.
• Support regulatory submissions.
• Plan, establish and maintain the effectiveness of company quality to meet regulatory expectations.
• Accountable for the company’s product quality and reliability to meet or exceed customer expectations.
• Liable for the company’s Quality Compliance to ensure compliance with regulatory agencies and all applicable standards worldwide.
• In support of the quality system, provide effective leadership support, training, and guidance to all company personnel.
• Write or guide employees in writing all company procedures, specifications, instructions, etc.
• Maintenance of the QA system.
• Periodic reports to Top management about Quality issues and analysis of MRB, CAPA, ECOs, internal and external audits, and product and process performance.
• Leading MRB, CAPA, and ECO committees.
• Responsible for the internal audit system.
• Subcontractor approval, auditing, and performance control.
• Establishment and management of product traceability systems (DMR).
• Responsible for approving the release of finished products.

Requirements

• Bachelor’s degree.
• At least 5 years of experience in the medical device industry.
• Multidisciplinary (mechanics, HW, SW) medical device experience is an advantage.
• Strong knowledge of design control regulations and standards (e.g., FDA, ISO 13485).
• Experienced with IEC60601, IEC6101001, and IEC 62304.
• Demonstrated expertise in leading design control activities, including risk management, verification/validation, and documentation.
• Excellent understanding of quality management systems and their application in the design process.
• Experience with internal and external audits related to design control and quality assurance.
• Strong analytical and problem-solving skills, with keen attention to detail. Excellent communication and interpersonal skills, with the ability to collaborate effectively across functions.
• Proficient in using standard MS Office applications.
• Fluent in English (oral and written).