דרושים הרקלס גיוס השמה

We are seeking a highly skilled Senior Project Manager to lead quality and regulatory projects in the medical device sector. The role involves delivering strong professional value to clients and managing projects across company offices, client sites, and remote settings.

Key Responsibilities
Manage quality and regulatory projects, ensuring alignment with scope, timelines, and budget.
Act as the main client interface, ensuring clear communication and high satisfaction.
Provide expert guidance on quality systems, regulatory requirements, and compliance standards.
Coordinate with cross-functional teams to deliver high-quality outcomes.
Promote continuous improvement and support operational excellence.

Join a well-established and innovative medical device company!
A unique opportunity to lead the lifecycle management of electronic systems for advanced medical devicesensuring regulatory compliance and delivering safe, high-quality products.
Key Responsibilities (Short Clear):

Prepare and review engineering documents, reports, specifications, and technical justifications in English.
Ensure proper use of system engineering, design controls, V V, and lifecycle processes.
Work closely with QA /RA teams to support audits, submissions, and documentation.
Collaborate with R D, manufacturing, quality, supply chain, and product teams for efficient development.
Participate in roadmaps, feasibility studies, and risk management.
Support design transfer, supplier evaluations, and sustaining engineering.
Communicate effectively with internal teams, partners, and regulatory bodies.

We are looking for an experienced and creative R D Engineer to join a small and dynamic team developing advanced medical device systems. This end-to-end role includes ideation, design, verification, regulatory support, and product transfer to manufacturing.

Role Overview (Short Clear):
Lead engineering tasks for multi-disciplinary medical devices (electronics, mechanics, software).
Design PCBs or provide technical oversight for electronic design.
Prepare product requirements, development documents, TEST specifications, and regulatory materials.
Collaborate with R D, QA, Manufacturing, RA, and suppliers.
Participate in V V, support transfer to manufacturing, and assist in problem-solving.
Drive engineering improvements to ensure performance, reliability, and compliance with FDA and quality standards.