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Principal Design Quality Engineer - New Product Development
Jobs Bostonscientific Com · Minnetonka, MN, US, 55343 · Remote · Deleted · $102,100–$194,000 / hour · SAP SuccessFactors RMK / CSB
Job facts
| Field | Value |
|---|---|
| Company | Jobs Bostonscientific Com |
| Title | Principal Design Quality Engineer - New Product Development |
| Normalized title | - |
| Department / team | - |
| Location | Minnetonka, MN, United States |
| Work model | Remote / Remote |
| Employment type | - |
| Salary | $102,100–$194,000 / hour |
| Status | deleted |
| ATS provider | SAP SuccessFactors RMK / CSB |
| Posted / first seen | 2026-06-01 / 2026-06-02 |
| Changed / last seen | 2026-06-19 / 2026-06-17 |
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| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Jobs Bostonscientific Com. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through SAP SuccessFactors RMK / CSB. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Minnetonka. | Open |
| Work model jobs | Active Remote postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Jobs Bostonscientific Com |
| Source | 4d1e650f-1002-4874-8aaf-3deab61c5dcc |
| ATS provider | SAP SuccessFactors RMK / CSB |
Description
Additional Location(s): US-MN-Minnetonka; US-MA-Marlborough
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.
About the Role
The Principal Design Quality Engineer will support the Valencia Technologies Integration project with a focus on New Product Development. This role is responsible for leading Design Assurance activities throughout the product development lifecycle, ensuring products and processes remain safe, effective, high quality, and compliant with Boston Scientific and global regulatory requirements.
Work Mode
At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work mode requiring employees to work onsite at least three days per week. This position is based in Minnetonka, MN or Marlborough, MA.
Relocation Assistance
Relocation assistance is available for this position.
Visa Sponsorship
Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position.
Key Responsibilities
Serve as the quality representative within cross-functional development teams, influencing project strategy, driving compliance to Design Control and Risk Management requirements, and ensuring alignment with regulatory and business objectives.
Lead Design Assurance activities throughout product development for an active implantable technology.
Apply sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality-related issues.
Author and maintain Design History File (DHF) documentation, including design inputs/outputs, technical rationales, verification/validation documentation, and risk management deliverables in compliance with internal and external requirements.
Lead and support product risk management activities throughout the product lifecycle, including hazard analysis, fault tree analysis, FMEA, usability risk assessments, and post-market risk evaluation.
Partner with R&D, Manufacturing, Regulatory, and other cross-functional teams to establish and implement Design Controls based on Risk Management, customer needs, and manufacturing inputs.
Support verification, validation, and usability testing activities to ensure products meet internal requirements, regulatory expectations, and customer needs.
Demonstrate strong working knowledge and application of validation methodologies, statistical techniques, and quality engineering principles.
Collaborate effectively within a mixed onsite and remote working environment.
Required Qualifications
Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline.
Minimum of 7+ years of experience in Design Assurance, Quality Engineering, New Product Development, or related medical device/regulated industry experience.
Strong understanding of FDA Quality System Regulation (21 CFR Part 820), ISO 13485, ISO 14971, and Design Control requirements for medical devices.
Demonstrated experience applying Quality Engineering tools and methodologies.
Strong verbal and written communication skills with the ability to influence across functions and levels.
Demonstrated experience authoring and reviewing detailed technical documentation.
Self-motivated with strong problem-solving skills and a bias for action.
Ability to effectively collaborate in a hybrid onsite and remote work environment.
Preferred Qualifications
Experience working with active implantable medical devices and/or medical electrical equipment.
Experience supporting acquisition integration and quality system harmonization activities.
Experience supporting software development lifecycle activities in accordance with IEC 62304.
Experience facilitating structured problem-solving methodologies and risk-based decision making.
Experience supporting regulatory inspections and external audits.
Adaptable and effective collaborator in both team-based and self-directed environments.
Requisition ID: 629871
Minimum Salary: $ 102100
Maximum Salary: $ 194000
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com— will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.
Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions : It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at
Full job record
| Job ID | 7edcdd0dc92d57122dbd16099afb5421dd10dc28 |
| Org ID | c7465584-6de9-4dd3-970e-6f24ea360e7f |
| Source ID | 4d1e650f-1002-4874-8aaf-3deab61c5dcc |
| Board ID | 4d1e650f-1002-4874-8aaf-3deab61c5dcc |
| Provider | successfactors_rmk |
| Provider Job Key | 1395768000 |
| Title | Principal Design Quality Engineer - New Product Development |
| Normalized Title | — |
| Status | deleted |
| Active | no |
| Location Text | Minnetonka, MN, US, 55343 |
| Department | — |
| Team | — |
| Employment Type | — |
| Workplace Type | remote |
| Remote Policy | remote |
| Country | United States |
| Region | MN |
| City | Minnetonka |
| Salary Raw | Additional Location(s): US-MN-Minnetonka; US-MA-Marlborough Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About the Role The Principal Design Quality Engineer will support the Valencia Technologies Integration project with a focus on New Product Development. This role is responsible for leading Design Assurance activities throughout the product development lifecycle, ensuring products and processes remain safe, effective, high quality, and compliant with Boston Scientific and global regulatory requirements. Work Mode At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work mode requiring employees to work onsite at least three days per week. This position is based in Minnetonka, MN or Marlborough, MA. Relocation Assistance Relocation assistance is available for this position. Visa Sponsorship Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position. Key Responsibilities Serve as the quality representative within cross-functional development teams, influencing project strategy, driving compliance to Design Control and Risk Management requirements, and ensuring alignment with regulatory and business objectives. Lead Design Assurance activities throughout product development for an active implantable technology. Apply sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality-related issues. Author and maintain Design History File (DHF) documentation, including design inputs/outputs, technical rationales, verification/validation documentation, and risk management deliverables in compliance with internal and external requirements. Lead and support product risk management activities throughout the product lifecycle, including hazard analysis, fault tree analysis, FMEA, usability risk assessments, and post-market risk evaluation. Partner with R&D, Manufacturing, Regulatory, and other cross-functional teams to establish and implement Design Controls based on Risk Management, customer needs, and manufacturing inputs. Support verification, validation, and usability testing activities to ensure products meet internal requirements, regulatory expectations, and customer needs. Demonstrate strong working knowledge and application of validation methodologies, statistical techniques, and quality engineering principles. Collaborate effectively within a mixed onsite and remote working environment. Required Qualifications Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline. Minimum of 7+ years of experience in Design Assurance, Quality Engineering, New Product Development, or related medical device/regulated industry experience. Strong understanding of FDA Quality System Regulation (21 CFR Part 820), ISO 13485, ISO 14971, and Design Control requirements for medical devices. Demonstrated experience applying Quality Engineering tools and methodologies. Strong verbal and written communication skills with the ability to influence across functions and levels. Demonstrated experience authoring and reviewing detailed technical documentation. Self-motivated with strong problem-solving skills and a bias for action. Ability to effectively collaborate in a hybrid onsite and remote work environment. Preferred Qualifications Experience working with active implantable medical devices and/or medical electrical equipment. Experience supporting acquisition integration and quality system harmonization activities. Experience supporting software development lifecycle activities in accordance with IEC 62304. Experience facilitating structured problem-solving methodologies and risk-based decision making. Experience supporting regulatory inspections and external audits. Adaptable and effective collaborator in both team-based and self-directed environments. Requisition ID: 629871 Minimum Salary: $ 102100 Maximum Salary: $ 194000 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com— will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). For MA positions : It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at |
| Salary Min | 102,100 |
| Salary Max | 194,000 |
| Salary Currency | USD |
| Salary Period | hour |
| Source URL | https://jobs.bostonscientific.com/job/Minnetonka-Principal-Design-Quality-Engineer-New-Product-Development-MN-55343/1395768000/ |
| Apply URL | /talentcommunity/apply/1395768000/?locale=en_US |
| First Seen At | 2026-06-02 13:00:55Z |
| Last Seen At | 2026-06-17 14:00:33Z |
| Last Checked At | 2026-06-19 14:09:03Z |
| Last Changed At | 2026-06-19 14:09:03Z |
| Inactive At | 2026-06-19 14:09:03Z |
| Source Posted At | 2026-06-01 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=successfactors_rmk/board=jobs.bostonscientific.com/date=2026-06-17/2026-06-17T13-59-58-664Z-765a342bfb0d970572df5db2e568bf8071e6d89902908a8a45c2962e214efc88.json |
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