COMPANY OVERVIEW

Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. We are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.
The Opportunity That Awaits You:
Are you ready to embark on an exciting journey with PROCEPT BioRobotics?
As we continue to grow and scale our operations team at PROCEPT, we have an excellent opportunity for a new Senior Supply Engineer who is Rresponsible for ensuring suppliers meet Procept’s requirements for quality, service, delivery, and cost. Drives suppliers to continuously improve business and manufacturing processes. Collaborates with Supplier Quality to evaluate and select suppliers. Guides R&D in choosing suppliers for new products and provides DFM input to new designs. Supports both NPI and on-going production, monitoring and working with suppliers to improve supplier performance. Executes detailed projects with suppliers to implement changes and improvements affecting quality, cost, capacity, risk, and sub-supplier management.
The ideal Candidate possesses broad and deep manufacturing experience for processes such as assembly of medical devices, machining, plastic injection molding experience etc.

THE QUALIFICATIONS WE NEED YOU TO POSSESS

• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• BS in Mechanical Engineering or equivalent with a minimum of seven years experience.
• Prior experience in the medical device industry is preferred.
• Experience in leading highly technical projects in a cross functional environment both internally and with CMs/Suppliers.
• Demonstrable knowledge in evaluating and challenging supplier technical, quality, and business capabilities.
• Extensive experience with root cause analysis and problem solving for both technical and process issues.
• Basic working knowledge of CAD (SolidWorks or other) software.
• Ability to read and interpret detailed mechanical drawings (GD&T) and communicate technical information.

THE QUALIFICATIONS WE WOULD LIKE YOU TO POSSESS

• Ability to interpret and understand the impact of purchased part changes like alternate raw material change, supplier process change, supplier tooling change, etc. to the internal manufacturing process and design, and develop, implement/execute qualification test case.
• Experience working in a structured design process such as ISO9000 or FDA QSR, knowledge of regulatory approval process and requirements.
• Working knowledge of design control and cGMP requirements for medical device manufacturing per FDA QSR and ISO13485-2003 or ISO9001 and EN46001, including experience in auditing suppliers to these standards.
• Ability to work in a cross functional environment, lead meetings, follow up on action items, deliverables in a timely manner and meeting deadlines. Escalate issues as and when necessary.
• Ability to travel to suppliers on an as needed basis – domestic and international

Please refer the Job description for details