Senior Manufacturing Engineer; Laser Welding

Company Overview

PROCEPT Bio Robotics is committed to revolutionizing treatment for benign prostatic hyperplasia (BPH) through innovation in surgical robotics. We put patients first and pursue continuous career growth for our people. Our culture values every employee, patient, and caregiver, fostering a collaborative environment that supports professional development and work‑life balance.

Join us as a Senior Manufacturing Engineer and lead the engineering of the Aquabeam Robotic System. You will develop new process technologies, drive continuous improvement, and support our mission to create best‑in‑class medical device manufacturing.

• Lead engineering support to manufacturing teams and resolve process and equipment issues.
• Develop training programs for operators and engineers.
• Define technology and equipment roadmaps for medical device technologies.
• Champion continuous improvement, identifying projects to maximize yield, capacity, and capability.
• Implement Design for Manufacturability (DFM) projects to reduce costs, improve processes, and enhance reliability.
• Design and evaluate fixtures, equipment, test methods, specifications, layouts, and standards.
• Maintain process documentation, including Manufacturing Instructions, Standard Work, PFMEA, and Control Plans.
• Collaborate with R&D and Process Development to develop weld schedules for new product transfers.
• Plan and execute new technical projects, determining scope, scale, and ROI.
• Build or procure improved fixtures, tooling, or equipment to increase quality, reliability, and yield.
• Provide engineering support to outside suppliers and contract manufacturers, ensuring quality and production targets are met.
• Train, develop, and provide direction to operators and technicians.
• Potential travel of up to 20% domestic and international.

• BS in an engineering discipline with a minimum of 5 years’ experience, or MS with a minimum of 3 years’ experience.
• Extensive root cause analysis and problem‑solving experience for technical and process issues.
• Experience with structured design processes such as ISO 9000 or FDA QSR, and knowledge of regulatory approval requirements.
• Working knowledge of design control and cGMP requirements for medical device manufacturing (FDA QSR, ISO 13485‑2003, ISO 9001, EN 46001).
• Basic CAD skills (e.g., Solid Works).

• Expertise in process technologies such as laser cutting, welding, brazing, and joining.
• Experience supporting medical device manufacturing.
• Experience leading highly technical cross‑functional projects, including with CMOs/vendors.
• Preferred Lean and Six Sigma skills.
• Advanced computer skills, including Microsoft Office and Solid Works proficiency.

$131,060 to $154,190