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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, and 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: At PROCEPT BioRobotics, you will be part of a team developing a surgical robot that combines real‑time data, multi‑dimensional imaging, and robotics to remove prostate tissue. As PROCEPT BioRobotics continues to expand, the Design Quality Assurance group requires a Failure Analysis Technician to support complaint investigations and root cause analysis. In this role, you will manage the failure analysis laboratory, perform device testing with advanced tools and capital equipment, and generate high‑quality documentation to support regulatory and audit requirements. You will work closely with cross‑functional engineering teams to analyze device failures, identify causes, and ensure accurate, compliant reporting.
What Your Day‑To‑Day Will Involve:
Managing the failure analysis laboratory, including handling devices exposed to bloodborne pathogens.
Maintaining a clean, organized, and compliant lab environment in accordance with safety, biosafety, and 5S lean principles.
Tracking and managing a high volume of devices through the failure analysis workflow, ensuring accurate labeling, chain‑of‑custody, and status tracking.
Performing detailed physical and functional testing on devices using advanced tools (e.g., oscilloscopes, data acquisition systems) as well as capital equipment test setups.
Conducting complaint and failure investigations, working closely with design, quality, and reliability engineers to identify root causes.
Documenting test protocols, results, and findings with precision, following Good Documentation Practices (GDP) and ensuring records are audit‑ready.
Writing clear, structured investigation reports that meet regulatory, quality system, and audit requirements.
Collaborating with engineers to analyze test outcomes and recommend potential next steps in root cause analysis.
Supporting continuous improvement by identifying gaps in lab processes, documentation, and equipment management.
Ensuring all test equipment is properly maintained, calibrated, and compliant with internal and external standards.
The Qualifications We Need You to Possess
High School Equivalent with 2‑year experience, or 1‑year technical degree/diploma with 1‑year experience in a laboratory, testing, or failure analysis environment.
Strong organizational skills with ability to manage multiple tasks simultaneously.
Knowledge of Good Documentation Practices (GDP) and experience writing technical reports that withstand regulatory and audit scrutiny.
Demonstrated experience in computer skills and comfort with basic Windows‑office software such as MS Word, Excel, PowerPoint, etc.
Ability to demonstrate technical problem solving and analytical skills.
The Qualifications We Would Like You to Possess
Familiarity with bloodborne pathogen (BBP) handling and biosafety practices.
Basic knowledge of mechanical and electronic concepts.
Hands‑on experience using test equipment (e.g., oscilloscope, multi‑meter, test logger, thermocouples, etc.).
Experience in medical device industry, particularly in a regulated environment (FDA QSR, ISO 13485, EU MDR).
Prior experience supporting complaint handling, CAPA, or reliability/failure analysis.
Familiarity with Lean/5S lab organization practices.
Experience with capital equipment, electromechanical systems, or robotics testing.
Working regularly in a laboratory environment while performing the duties of this job.
Salary and Benefits
$69,000 – $81,000 a year, including an annual bonus of 10%, RSUs at offer, and non‑exempt role.
For US‑Based Candidates Only. Work Authorization Status: Citizen / Permanent Resident.
Understanding PROCEPT's Culture At PROCEPT, we believe every person matters. Every employee, every patient, every caregiver. We create a revolution through innovation, curiosity, ingenuity, and conviction in the power of technology to transform lives. We value humility, engagement, and seamless teamwork toward a common goal. Our live induction program and unique management development initiatives cultivate camaraderie, skill enhancement, and shared purpose. Join a community devoted to making a difference.
BENEFITS OF WORKING AT PROCEPT! PROCEPT offers comprehensive health and wellness benefits: full medical coverage, wellness programs, on‑site gym, 401(k) plan with employer match, short‑term and long‑term disability coverage, basic life insurance, wellbeing benefits, flexible or paid time off, paid parental leave, paid holidays, and more.
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT PROCEPT BioRobotics is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind on the basis of race, color, national origin, religion, gender, gender identity, sexual orientation, disability, genetic information, pregnancy, age, or any other protected status set forth in federal, state, or local laws. This policy applies to all employment practices within our organization.
PAY RANGE TRANSPARENCY Procept is committed to fair and equitable compensation practices. The pay range(s) for this role represent a base salary range for non‑commissionable roles or on‑target earnings for commissionable roles. Actual compensation packages are based on factors unique to each candidate, including job‑related skills, depth of experience, relevant certifications and training, and specific work location. The total compensation package for this position may also include eligibility for annual performance bonus, equity, and the benefits listed above.
WORK ENVIRONMENT We’ll provide training and require maintenance of trained status for all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance. You are also expected to understand and adhere to PROCEPT BioRobotics Quality & EHS policies.
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The Opportunity That Awaits You: At PROCEPT BioRobotics, you will be part of a team developing a surgical robot that combines real‑time data, multi‑dimensional imaging, and robotics to remove prostate tissue. As PROCEPT BioRobotics continues to expand, the Design Quality Assurance group requires a Failure Analysis Technician to support complaint investigations and root cause analysis. In this role, you will manage the failure analysis laboratory, perform device testing with advanced tools and capital equipment, and generate high‑quality documentation to support regulatory and audit requirements. You will work closely with cross‑functional engineering teams to analyze device failures, identify causes, and ensure accurate, compliant reporting.
What Your Day‑To‑Day Will Involve:
Managing the failure analysis laboratory, including handling devices exposed to bloodborne pathogens.
Maintaining a clean, organized, and compliant lab environment in accordance with safety, biosafety, and 5S lean principles.
Tracking and managing a high volume of devices through the failure analysis workflow, ensuring accurate labeling, chain‑of‑custody, and status tracking.
Performing detailed physical and functional testing on devices using advanced tools (e.g., oscilloscopes, data acquisition systems) as well as capital equipment test setups.
Conducting complaint and failure investigations, working closely with design, quality, and reliability engineers to identify root causes.
Documenting test protocols, results, and findings with precision, following Good Documentation Practices (GDP) and ensuring records are audit‑ready.
Writing clear, structured investigation reports that meet regulatory, quality system, and audit requirements.
Collaborating with engineers to analyze test outcomes and recommend potential next steps in root cause analysis.
Supporting continuous improvement by identifying gaps in lab processes, documentation, and equipment management.
Ensuring all test equipment is properly maintained, calibrated, and compliant with internal and external standards.
The Qualifications We Need You to Possess
High School Equivalent with 2‑year experience, or 1‑year technical degree/diploma with 1‑year experience in a laboratory, testing, or failure analysis environment.
Strong organizational skills with ability to manage multiple tasks simultaneously.
Knowledge of Good Documentation Practices (GDP) and experience writing technical reports that withstand regulatory and audit scrutiny.
Demonstrated experience in computer skills and comfort with basic Windows‑office software such as MS Word, Excel, PowerPoint, etc.
Ability to demonstrate technical problem solving and analytical skills.
The Qualifications We Would Like You to Possess
Familiarity with bloodborne pathogen (BBP) handling and biosafety practices.
Basic knowledge of mechanical and electronic concepts.
Hands‑on experience using test equipment (e.g., oscilloscope, multi‑meter, test logger, thermocouples, etc.).
Experience in medical device industry, particularly in a regulated environment (FDA QSR, ISO 13485, EU MDR).
Prior experience supporting complaint handling, CAPA, or reliability/failure analysis.
Familiarity with Lean/5S lab organization practices.
Experience with capital equipment, electromechanical systems, or robotics testing.
Working regularly in a laboratory environment while performing the duties of this job.
Salary and Benefits
$69,000 – $81,000 a year, including an annual bonus of 10%, RSUs at offer, and non‑exempt role.
For US‑Based Candidates Only. Work Authorization Status: Citizen / Permanent Resident.
Understanding PROCEPT's Culture At PROCEPT, we believe every person matters. Every employee, every patient, every caregiver. We create a revolution through innovation, curiosity, ingenuity, and conviction in the power of technology to transform lives. We value humility, engagement, and seamless teamwork toward a common goal. Our live induction program and unique management development initiatives cultivate camaraderie, skill enhancement, and shared purpose. Join a community devoted to making a difference.
BENEFITS OF WORKING AT PROCEPT! PROCEPT offers comprehensive health and wellness benefits: full medical coverage, wellness programs, on‑site gym, 401(k) plan with employer match, short‑term and long‑term disability coverage, basic life insurance, wellbeing benefits, flexible or paid time off, paid parental leave, paid holidays, and more.
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT PROCEPT BioRobotics is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind on the basis of race, color, national origin, religion, gender, gender identity, sexual orientation, disability, genetic information, pregnancy, age, or any other protected status set forth in federal, state, or local laws. This policy applies to all employment practices within our organization.
PAY RANGE TRANSPARENCY Procept is committed to fair and equitable compensation practices. The pay range(s) for this role represent a base salary range for non‑commissionable roles or on‑target earnings for commissionable roles. Actual compensation packages are based on factors unique to each candidate, including job‑related skills, depth of experience, relevant certifications and training, and specific work location. The total compensation package for this position may also include eligibility for annual performance bonus, equity, and the benefits listed above.
WORK ENVIRONMENT We’ll provide training and require maintenance of trained status for all relevant aspects of the PROCEPT BioRobotics Quality Management System to ensure product and support regulatory compliance. You are also expected to understand and adhere to PROCEPT BioRobotics Quality & EHS policies.
#J-18808-Ljbffr