Procept Biorobotics2mo ago

USD 144000–169790/yr

Staff Quality Compliance Engineer

United States·San JoseFull-Timelead

OtherCompliance Engineer

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Quick Summary

Overview

Company Overview Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH,…

Technical Tools

people-management

Company Overview

Embark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and 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:

Reporting to the Senior Director, Global Quality Compliance and PMS, the Staff Quality Engineer, Quality Compliance will devise and lead execution of meaningful actions to improve the compliance, effectiveness, and efficiencies of processes within the Quality Compliance and PMS function. This role will represent Quality Compliance and PMS when partnering with internal department and cross-functional stakeholders and process owners. Develop and implement Quality tools to monitor key quality metrics that reflect health of the Quality System and identify opportunities for continuous improvement to scale workflows in support of evolving business needs.

Lead and manage special projects for the Quality Compliance and Post-Market Surveillance team, including planning, execution, and delivery of strategic initiatives and continuous improvement efforts.

Proactively identify process risks and improvement opportunities within the Quality Management System (QMS), leveraging a deep understanding of cross-functional interdependencies to implement sustainable, effective solutions.

Serve as a Quality Compliance and Post-Market Surveillance team representative on cross-functional initiatives, operating independently while influencing stakeholders and coordinating activities to meet project objectives.

Perform and lead Corrective and Preventive Actions (CAPA), including conducting thorough root cause investigations and developing corrective actions with appropriate scope and rigor relative to the identified quality issue.

Define key performance requirements for processes and projects; establish monitoring mechanisms and evaluate effectiveness against defined objectives to ensure continuous improvement.

Review and interpret regulations, standards, and guidance to ensure products, processes, and services remain compliant and aligned with state-of-the-art and regulatory expectations.

Apply sound technical judgment, data-driven analysis, and pragmatic problem-solving within the constraints of applicable regulations, standards, and internal procedures.

Drive cross-functional collaboration by effectively engaging subject matter experts and stakeholders to achieve aligned, timely outcomes.

Demonstrate leadership through technical competence, influence, accountability, and independent decision-making, without direct people management responsibility.

Maintain trained status and comply with the PROCEPT BioRobotics Quality Management System (QMS) and EHS policies.

Perform other duties as assigned.

Bachelor’s degree in engineering, science, or another technical discipline.

8 years of progressive experience in a medical device industry, including at least 5 years in quality systems, quality engineering, and/or compliance roles.

Working knowledge of FDA QSR/QMSR, ISO 13485, MDSAP, and EU MDR regulatory requirements.

Working knowledge of computer software validation principles, including in-device software, GxP systems, and 21 CFR Part 11.

Demonstrated ability to lead project teams and deliver results within aggressive timelines.

Strong analytical, organizational, and problem-solving skills.

Excellent written and verbal communication skills, with the ability to clearly convey complex concepts to diverse audiences.

Ability to apply conceptual and systems thinking to understand complex issues and downstream implications.

Proven ability to collaborate effectively in a fast-paced, matrixed environment.

Ability to travel up to 10% as required.

Master’s degree in engineering, science, or another technical discipline.

Prior supervisory or managerial experience.

Location & Eligibility

Where is the job

San Jose, United States

Hybrid — some on-site time required

Who can apply

Listing Details

Posted: March 2, 2026
First seen: April 29, 2026
Last seen: May 12, 2026

Posting Health

Days active: 9
Repost count: 0
Trust Level: 44%
Scored at: May 9, 2026

Signal breakdown

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Procept Biorobotics

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PROCEPT BioRobotics is a leading surgical robotics company focused on advancing urological care with groundbreaking solutions like the HYDROS Robotic System for Aquablation therapy.

Employees

750

Founded

2007

Domain

procept-biorobotics.com

Jobs

View 62 jobs

View company profile

Salary

USD 144000–169790

per year