Senior Quality Engineer Disposables
San Jose, CA - USA
Job Summary
The Opportunity That Awaits You:
Do you want to be part of an innovative cutting-edge technology and robotics company that is transforming the treatment of BPH Are you excited to work with an enthusiastic driven and collaborative team that continuously learns and improves together Are you a leader who is passionate about driving process excellence and making a meaningful impact Are you detail-oriented and thrive in a fast-paced NPI environment
At PROCEPT BioRobotics you will have the opportunity to contribute to our continuous improvement culture as part of our Quality Engineering team supporting New Product Introduction (NPI) for Disposables and Accessories. As a Senior Quality Engineer you will play a critical role in ensuring the quality reliability and scalability of our single-use products and accessory components from development through commercialization.
In this role you will partner cross-functionally with R&D Manufacturing Regulatory and Supply Chain teams to support product development design transfer and production readiness. You will help establish and maintain robust quality systems and processes in compliance with FDA Quality System Regulation (QSR) ISO 13485 and EU MDR. A detail-oriented proactive and solutions-driven mindset along with the ability to independently manage priorities in a dynamic NPI environment will be key to success in this position.
What Your Day-To-Day Will Involve:
- Lead and contribute to the planning and execution of design controls risk management and design verification/validation (V&V) for new products.
- Develop maintain and support the Design History File (DHF) ensuring complete compliance with internal Quality Management System (QMS) processes and external regulatory standards.
- Partner closely with R&D engineering to clearly define design inputs design outputs and comprehensive traceability matrices.
- Drive the strategy and execution of risk-based design verification and validation testing.
- Spearhead the development of the Risk Management File (per ISO 14971) analyzing and assessing risks associated with the user design manufacturing process and supply chain.
- Ensure that robust reliable and scalable designs are successfully transferred to manufacturing environments. Review early-stage designs material selections technical requirements and engineering drawings for manufacturability and quality.
- Evaluate and assess Verification & Validation (V&V) failures perform root cause analysis and drive Non conformances (NCMRs) corrective and preventive actions (CAPA) to ensure product quality and compliance
- Collaborate with Regulatory Affairs to provide vital technical data and documentation for regulatory submissions (e.g. 510(k) MDR) and actively respond to agency submission questions.
- Support internal and external audits including preparation and direct interaction with auditors.
- Demonstrates knowledge of biocompatibility sterilization methods (EO VHP) atmospheric conditioning and transit testing with the ability to perform change assessments
- Knowledge of reprocessing reusable medical devices is a plus.
- Maintain trained status for and comply with all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance.
- Ability to support/lead department projects and perform other work-related duties as assigned
The Qualifications We Need You to Possess
- BS in Engineering Microbiology Life Sciences or related technical field (MS preferred)
- Minimum 5 years of experience in medical device industry (class II medical devices preferred)
- Direct experience working with surgical instruments electromechanical devices or surgical accessories is highly preferred.
- Strong understanding of FDA 21 CFR Part 820 ISO 13485 ISO 14971 and EU MDR.
- Self-starter with ability to lead in a fast-paced environment with ability to prioritize and manage multiple projects.
- Proficient in statistical methods and tools such as Minitab to support validation and quality decisions.
- Strong leadership in initiating improvement discussions and driving team success.
The Qualifications We Would Like You to Possess
- Knowledge of biocompatibility (ISO 10993) and biological risk assessment are a plus.
- Knowledge of Reprocessing validations of reusable medical devices is a plus
For US-Based Candidates Only
Work Authorization Status: Citizen / Permanent Resident
For this role the anticipated base pay range is $per year.
Plus eligibility for an annual bonus and equity/RSUs
Required Experience:
Senior IC
About Company
PROCEPT BioRobotics is a surgical robotics company focused on advancing patient care by developing transformative solutions in urology.