Johnson & Johnson MedTech
Sr. Quality Engineer- Shockwave Medical
Johnson & Johnson MedTech, Santa Clara, California, us, 95053
Sr. Quality Engineer – Shockwave Medical
Johnson & Johnson MedTech is hiring a Sr. Quality Engineer for Shockwave Medical Inc. located in Santa Clara, CA. Apply via the Johnson & Johnson careers site.
Position Overview: The Sr. Quality Engineer will support manufacturing and work cross‑functionally to resolve technical problems. Participates in decisions on scope of work, risk management, design changes, process improvements, material disposition, and implementation of revised specifications. Provides and develops solutions to broad problems, accomplishes complex assignments, develops protocols for design, and/or process activities, (including those related to verification or validation activities), determines criteria and subsequently generates summary (or final) reports.
Essential Job Functions
Responsible for developing, applying, revising and maintaining quality standards for processing materials/products into partially or finished products.
Designs and implements methods and/or procedures for inspecting, testing and evaluating the precision and accuracy of products, components, sub‑assemblies and/or production equipment.
Analyzes nonconformance reports and returned products and recommends corrective action.
Prepares documentation for inspection/testing procedures, development studies, validation protocols and reports, quality plans, product defect investigations and inspection plans. Must be able to write a technical document with sufficient clarity, detail and correctness to be submitted for regulatory review with confidence. Must be able to review and provide value‑added feedback to others writing such documents.
Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments.
Plans and conducts work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria. Provides guidance to manufacturing and development engineers regarding documentation, process controls, data feedback systems, and best quality practices.
Independently performs most assignments with an understanding of the overall expectations. Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects.
Plans, schedules, conducts, and coordinates detailed phases of engineering work in part of a major project.
Performs work which involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.
Work requires a broad knowledge of precedents in the specialty area and a good knowledge of principles and practices of related specialties. Familiarity with FDA guidance documents and ISO and ASTM standards related to quality and medical device industry is an asset.
Independently assesses if components, sub‑assemblies, products meet specification and can initiate, investigate and resolve non‑conformances by working in conjunction with a multi‑disciplinary team.
Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Responsible for participating in design reviews and pre‑validation assessments to ensure the safe and environmentally sound start‑up of new processes, and ensure the process has adequate and appropriate process controls. Responsible for participating and/or taking lead role in developing the risk management plan for new projects transitioning into manufacturing (Hazard assessment, design trace matrix development, DV&V testing, and FMEA).
May technically supervise or coordinate the work of engineers, technicians, and others who assist in specific assignments.
Practices company safety, quality policies and procedures, and actively requires conformance.
May conduct internal and supplier audits. Certified as a lead auditor in ISO13485:2016 would be an asset. Familiarity with IEC 60601 and IEC 62304 is an asset.
Processing, investigating, and completing customer complaints, which could require direct email responses to customers.
Composes technical complaint reports timely and accurately based on reported information and device investigation data.
Responsible for developing and maintaining calibration requirements for tools and equipment in the R&D, Manufacturing, and Quality areas.
Knowledge of statistics and Minitab, including process capability and data normality assessments, analysis of variance, hypothesis testing, determining appropriate sample sizes, tolerance interval assessments for variable and attribute data, design of experiment (DOE), and variable and attribute sampling plan applications would be a great asset.
Other duties as assigned.
Requirements
BS in a related engineering discipline and 5+ years of related experience; or MS in a related engineering discipline and 3+ years of related experience.
Experience in the medical device industry is highly preferred.
Strong technical writing skills are required.
Experience in customer complaint investigations and complaint report writing.
Experience in manufacturing support as a Quality Engineer.
Must be proactive, self‑motivated, and work independently with minimal supervision.
Experience with balloon catheters, automated machines and electrical systems with software validation is strongly preferred.
Experience with Extrusion and Braiding is a plus.
Experience in completing Medical Device Reports (MDR) and Vigilance (MDV) submissions is an asset.
Experience in writing and reviewing design verification and validation protocols.
Preferred experience in generating documentation and criteria for validation of manufacturing line transfer to alternative sites.
Certification and/or license in a specific discipline would be an asset.
Certified Quality Engineer would be an asset.
Must be willing to travel up to 10% of the time.
Effective communication skills with all levels of management and organizations.
Operate independently and adaptability to changing requirements.
Ability to work in a fast‑paced environment, managing multiple priorities.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is : $91,000.00 – $147,200.00
Benefits Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year (48 hours for Colorado residents, 56 hours for Washington residents)
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52‑week rolling period (10 days)
Volunteer Leave – 32 hours per calendar year
Military Spouse Time‑Off – 80 hours per calendar year
For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits
Seniority Level Not Applicable
Employment Type Full‑time
Job Function Quality Assurance
Industries Hospitals and Health Care
Location Santa Clara, CA
Referrals increase your chances of interviewing at Johnson & Johnson MedTech by 2x.
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Position Overview: The Sr. Quality Engineer will support manufacturing and work cross‑functionally to resolve technical problems. Participates in decisions on scope of work, risk management, design changes, process improvements, material disposition, and implementation of revised specifications. Provides and develops solutions to broad problems, accomplishes complex assignments, develops protocols for design, and/or process activities, (including those related to verification or validation activities), determines criteria and subsequently generates summary (or final) reports.
Essential Job Functions
Responsible for developing, applying, revising and maintaining quality standards for processing materials/products into partially or finished products.
Designs and implements methods and/or procedures for inspecting, testing and evaluating the precision and accuracy of products, components, sub‑assemblies and/or production equipment.
Analyzes nonconformance reports and returned products and recommends corrective action.
Prepares documentation for inspection/testing procedures, development studies, validation protocols and reports, quality plans, product defect investigations and inspection plans. Must be able to write a technical document with sufficient clarity, detail and correctness to be submitted for regulatory review with confidence. Must be able to review and provide value‑added feedback to others writing such documents.
Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments.
Plans and conducts work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria. Provides guidance to manufacturing and development engineers regarding documentation, process controls, data feedback systems, and best quality practices.
Independently performs most assignments with an understanding of the overall expectations. Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects.
Plans, schedules, conducts, and coordinates detailed phases of engineering work in part of a major project.
Performs work which involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.
Work requires a broad knowledge of precedents in the specialty area and a good knowledge of principles and practices of related specialties. Familiarity with FDA guidance documents and ISO and ASTM standards related to quality and medical device industry is an asset.
Independently assesses if components, sub‑assemblies, products meet specification and can initiate, investigate and resolve non‑conformances by working in conjunction with a multi‑disciplinary team.
Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Responsible for participating in design reviews and pre‑validation assessments to ensure the safe and environmentally sound start‑up of new processes, and ensure the process has adequate and appropriate process controls. Responsible for participating and/or taking lead role in developing the risk management plan for new projects transitioning into manufacturing (Hazard assessment, design trace matrix development, DV&V testing, and FMEA).
May technically supervise or coordinate the work of engineers, technicians, and others who assist in specific assignments.
Practices company safety, quality policies and procedures, and actively requires conformance.
May conduct internal and supplier audits. Certified as a lead auditor in ISO13485:2016 would be an asset. Familiarity with IEC 60601 and IEC 62304 is an asset.
Processing, investigating, and completing customer complaints, which could require direct email responses to customers.
Composes technical complaint reports timely and accurately based on reported information and device investigation data.
Responsible for developing and maintaining calibration requirements for tools and equipment in the R&D, Manufacturing, and Quality areas.
Knowledge of statistics and Minitab, including process capability and data normality assessments, analysis of variance, hypothesis testing, determining appropriate sample sizes, tolerance interval assessments for variable and attribute data, design of experiment (DOE), and variable and attribute sampling plan applications would be a great asset.
Other duties as assigned.
Requirements
BS in a related engineering discipline and 5+ years of related experience; or MS in a related engineering discipline and 3+ years of related experience.
Experience in the medical device industry is highly preferred.
Strong technical writing skills are required.
Experience in customer complaint investigations and complaint report writing.
Experience in manufacturing support as a Quality Engineer.
Must be proactive, self‑motivated, and work independently with minimal supervision.
Experience with balloon catheters, automated machines and electrical systems with software validation is strongly preferred.
Experience with Extrusion and Braiding is a plus.
Experience in completing Medical Device Reports (MDR) and Vigilance (MDV) submissions is an asset.
Experience in writing and reviewing design verification and validation protocols.
Preferred experience in generating documentation and criteria for validation of manufacturing line transfer to alternative sites.
Certification and/or license in a specific discipline would be an asset.
Certified Quality Engineer would be an asset.
Must be willing to travel up to 10% of the time.
Effective communication skills with all levels of management and organizations.
Operate independently and adaptability to changing requirements.
Ability to work in a fast‑paced environment, managing multiple priorities.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is : $91,000.00 – $147,200.00
Benefits Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year (48 hours for Colorado residents, 56 hours for Washington residents)
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52‑week rolling period (10 days)
Volunteer Leave – 32 hours per calendar year
Military Spouse Time‑Off – 80 hours per calendar year
For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits
Seniority Level Not Applicable
Employment Type Full‑time
Job Function Quality Assurance
Industries Hospitals and Health Care
Location Santa Clara, CA
Referrals increase your chances of interviewing at Johnson & Johnson MedTech by 2x.
#J-18808-Ljbffr