Intuitive
Join to apply for the
Quality Engineer 3
role at
Intuitive Join to apply for the
Quality Engineer 3
role at
Intuitive This range is provided by Intuitive. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$107,000.00/yr - $181,100.00/yr Company Description
Job Description
Primary Function of Position
As Intuitive’s da Vinci Surgical System becomes adopted by an increasing population of hospitals, surgeons and patients, we are building a focused team to drive reliability, quality, and safety to ever-better levels. This focus applies to product in use, product in manufacturing, and product in design. Help us powerfully drive our quality mission in our young and growing company by bringing your hands-on experience in solving tough engineering problems, your fascination with complex electro-mechanical devices, and your passion for the best practices to design, monitor, and improve product and process.
The position is a Quality Engineer-3 based out of Peachtree corners, GA and will support manufacturing and remanufacturing of systems for the Davinci Multiport (MP) business unit.
Essential Job Duties
Initial roles and responsibilities for this position will include the following: 60% involvement in supporting sustaining manufacturing operations, 25% design controls and 15% quality advocacy (quality improvements). Manufacturing support: Support manufacturing processes, including failure analysis, documentation review and approval, tooling qualification, and defect containments. Ensure manufacturing activities follow ISI procedures and regulations. Support development and execution of process validation and verification test plans, protocols, and reports. Maintain site level process FMEA and risk management files and update as required. Support production ramp and work cross functionally on issue and support continuous improvement projects. Support investigation and disposition of non-conformances, both internal and supplier related. Product development: Support various product and subsystem type design changes (not a full design quality support) Participate in risk management process ensuring that the essential performance aspects are correctly mitigated in the product quality plans. Ensure design changes are established and implemented according to ISI standards and applicable regulations. Recommend design processes and methods to meet quality goals (DFX, etc.). Quality Advocacy: Develop and apply corporate-level quality metrics. Ensure the quality system requirements are effectively established and maintained. Lead and manage quality initiatives in one or more areas of product and processes quality. Evaluates deviations and non-conformances and supports resolution of quality issues Supports process validation and verification. Perform risk analysis and determines quality disposition for variance requests and non-conformances Represents the department cross-functionally in meetings that may include senior and external personnel Releases process and document changes through engineering change orders and deviations using ISI change control process Escalates to direct management all quality issues that could impact patient safety or surgical efficacy Ensures successful, on-time completion of department projects, communicates constraints to direct management when successful project completion is at risk. Performs other duties as assigned by the management.
Qualifications
Required Skills and Experience
Competency Requirements: In order to adequately perform the responsibilities of this position the individual must possess: Education: Bachelor degree in electrical, mechanical or system engineering, math, or physics. Advanced degree preferred. 4+ years of relevant experience in medical device or manufacturing environment. Demonstrated proficiencies of CFR 21 820/ ISO 13485 requirements for making process or design changes. Understands product risk management, experience in generate FMEA and process FMEA. Understands Design Controls, Change Controls, Product, and Engineering Processes. Proficient with generate and execute Qualification and Validation protocol and Quality Assurance Procedures. Experienced in leading product containment and rework activities. Proficient in SPC & Six Sigma methodology and tools (e.g. uses DMAIC process and basic tools such as 5 Why's, control charts, fishbone diagram). Understands typical Excel data analysis operations (e.g. Vlookup, Pivot table and pivot chart functions) Able to create Multi-source report, trends, and interprets data with minimal oversight. Capable of thinking independently and make decision based on limited information. Ability to communicate effectively both verbally and in writing Integrity: Accepting and adhering to high ethical, moral, and personal dealing with others values in decisions, communications, actions, and when Dealing with others Ability to work independently and handle tasks with competing priorities effectively.
Additional Information
Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.
Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.
Mandatory Notices
We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.
Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee.
We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target salary ranges are listed.
Base Salary Range Region 1: $125,900 - $181,100
Base Salary Range Region 2:
$107,000 - $154,000
Shift:
Day
Travel:
10% of the time
Workplace Type:
Onsite - This job is fully onsite. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Quality Assurance Industries Medical Equipment Manufacturing Referrals increase your chances of interviewing at Intuitive by 2x Sign in to set job alerts for “Quality Engineer” roles.
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Quality Engineer 3
role at
Intuitive Join to apply for the
Quality Engineer 3
role at
Intuitive This range is provided by Intuitive. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$107,000.00/yr - $181,100.00/yr Company Description
Job Description
Primary Function of Position
As Intuitive’s da Vinci Surgical System becomes adopted by an increasing population of hospitals, surgeons and patients, we are building a focused team to drive reliability, quality, and safety to ever-better levels. This focus applies to product in use, product in manufacturing, and product in design. Help us powerfully drive our quality mission in our young and growing company by bringing your hands-on experience in solving tough engineering problems, your fascination with complex electro-mechanical devices, and your passion for the best practices to design, monitor, and improve product and process.
The position is a Quality Engineer-3 based out of Peachtree corners, GA and will support manufacturing and remanufacturing of systems for the Davinci Multiport (MP) business unit.
Essential Job Duties
Initial roles and responsibilities for this position will include the following: 60% involvement in supporting sustaining manufacturing operations, 25% design controls and 15% quality advocacy (quality improvements). Manufacturing support: Support manufacturing processes, including failure analysis, documentation review and approval, tooling qualification, and defect containments. Ensure manufacturing activities follow ISI procedures and regulations. Support development and execution of process validation and verification test plans, protocols, and reports. Maintain site level process FMEA and risk management files and update as required. Support production ramp and work cross functionally on issue and support continuous improvement projects. Support investigation and disposition of non-conformances, both internal and supplier related. Product development: Support various product and subsystem type design changes (not a full design quality support) Participate in risk management process ensuring that the essential performance aspects are correctly mitigated in the product quality plans. Ensure design changes are established and implemented according to ISI standards and applicable regulations. Recommend design processes and methods to meet quality goals (DFX, etc.). Quality Advocacy: Develop and apply corporate-level quality metrics. Ensure the quality system requirements are effectively established and maintained. Lead and manage quality initiatives in one or more areas of product and processes quality. Evaluates deviations and non-conformances and supports resolution of quality issues Supports process validation and verification. Perform risk analysis and determines quality disposition for variance requests and non-conformances Represents the department cross-functionally in meetings that may include senior and external personnel Releases process and document changes through engineering change orders and deviations using ISI change control process Escalates to direct management all quality issues that could impact patient safety or surgical efficacy Ensures successful, on-time completion of department projects, communicates constraints to direct management when successful project completion is at risk. Performs other duties as assigned by the management.
Qualifications
Required Skills and Experience
Competency Requirements: In order to adequately perform the responsibilities of this position the individual must possess: Education: Bachelor degree in electrical, mechanical or system engineering, math, or physics. Advanced degree preferred. 4+ years of relevant experience in medical device or manufacturing environment. Demonstrated proficiencies of CFR 21 820/ ISO 13485 requirements for making process or design changes. Understands product risk management, experience in generate FMEA and process FMEA. Understands Design Controls, Change Controls, Product, and Engineering Processes. Proficient with generate and execute Qualification and Validation protocol and Quality Assurance Procedures. Experienced in leading product containment and rework activities. Proficient in SPC & Six Sigma methodology and tools (e.g. uses DMAIC process and basic tools such as 5 Why's, control charts, fishbone diagram). Understands typical Excel data analysis operations (e.g. Vlookup, Pivot table and pivot chart functions) Able to create Multi-source report, trends, and interprets data with minimal oversight. Capable of thinking independently and make decision based on limited information. Ability to communicate effectively both verbally and in writing Integrity: Accepting and adhering to high ethical, moral, and personal dealing with others values in decisions, communications, actions, and when Dealing with others Ability to work independently and handle tasks with competing priorities effectively.
Additional Information
Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.
Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.
Mandatory Notices
We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.
Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee.
We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target salary ranges are listed.
Base Salary Range Region 1: $125,900 - $181,100
Base Salary Range Region 2:
$107,000 - $154,000
Shift:
Day
Travel:
10% of the time
Workplace Type:
Onsite - This job is fully onsite. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Quality Assurance Industries Medical Equipment Manufacturing Referrals increase your chances of interviewing at Intuitive by 2x Sign in to set job alerts for “Quality Engineer” roles.
Quality Engineer (Level 1 or 2) - Automotive Manufacturing
Atlanta, GA $70,000.00-$85,000.00 3 weeks ago Quality Engineer (Level 1 or 2) - Automotive Manufacturing
Supplier Quality Engineer II (Hybrid - Kennesaw, GA)
Advanced Quality Engineer (Clarkston, GA)*
Clarkston, GA $122,292.00-$149,468.00 6 days ago Supplier Quality Engineer level I or II - automotive
Atlanta, GA $88,600.00-$181,900.00 3 days ago Supplier Quality Engineer level I or II - automotive
Atlanta, GA $85,000.00-$140,000.00 4 days ago Clarkston, GA $98,413.00-$120,282.00 1 month ago Manufacturing Engineer JN -052025-160793
Atlanta, GA $80,000.00-$100,000.00 1 week ago Sr. Supplier Quality Engineer, Intelligence Systems
Atlanta, GA $142,000.00-$213,000.00 2 weeks ago QA Systems Engineer – IATF 16949 QMS and audit certified
Quality Control Engineer, Integrated Project Quality (IPQ)
Sr. Engineer- Supplier Quality (Atlanta/Germantown)
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr