The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will support Audit ...
The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will support Audit ...
The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will support Audit ...
The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will support Audit ...
The Senior Quality Systems Engineer will provide dedicated ownership and execution support for quality systems, QMS platform enablement, executive reporting, and supplier quality initiatives. This ...
The Senior Quality Systems Engineer will provide dedicated ownership and execution support for quality systems, QMS platform enablement, executive reporting, and supplier quality initiatives. This ...
Quality System Engineer III
Maple Grove, MN · On-site
$78K - $148K/yr
Create Alert The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will ...
Quality System Engineer III
Maple Grove, MN · On-site
$78K - $148K/yr
Create Alert The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will ...
Principal Quality System Engineer - CAPA
Maple Grove, MN · On-site
$102K - $194K/yr
Create Alert Principal Quality System Engineer - CAPA Onsite Location(s): Maple Grove, MN, US, 55311 Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer ...
Principal Quality System Engineer - CAPA
Maple Grove, MN · On-site
$102K - $194K/yr
Create Alert Principal Quality System Engineer - CAPA Onsite Location(s): Maple Grove, MN, US, 55311 Principal Quality System Engineer - CAPA About the role: As a Principal Quality System Engineer ...
$78K - $148K/yr
Create Alert The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will ...
$78K - $148K/yr
Create Alert The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will ...
Senior Quality System Engineer
Costa Mesa, CA · On-site
$94K - $128K/yr
ABOUT THE TEAM Anduril's Quality organization is seeking a Senior Quality System Engineer to join our team and help develop future opportunities for our internal quality management system and ...
Senior Quality System Engineer
Costa Mesa, CA · On-site
$94K - $128K/yr
ABOUT THE TEAM Anduril's Quality organization is seeking a Senior Quality System Engineer to join our team and help develop future opportunities for our internal quality management system and ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
As a Principal Quality System Engineer supporting CAPA, you will serve as a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements of the Corrective ...
We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery ... Minimum 12 years of compliance, quality systems, or regulatory program experience, or equivalent ...
We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery ... Minimum 12 years of compliance, quality systems, or regulatory program experience, or equivalent ...
The Quality Systems Manager will be responsible for managing a staff of quality system ... Minimum of 5 years of relevant quality engineering experience in the medical device or ...
The Quality Systems Manager will be responsible for managing a staff of quality system ... Minimum of 5 years of relevant quality engineering experience in the medical device or ...
Quality System Specialist
Saint Paul, MN · On-site
$70K - $82K/yr
Collaborate with Manufacturing, Engineering, Quality Assurance, Regulatory Affairs, and Operations personnel to ensure consistent application of quality system requirements. * Identify opportunities ...
Quality System Specialist
Saint Paul, MN · On-site
$70K - $82K/yr
Collaborate with Manufacturing, Engineering, Quality Assurance, Regulatory Affairs, and Operations personnel to ensure consistent application of quality system requirements. * Identify opportunities ...
Quality System Manager
Maple Grove, MN · On-site
The Quality Systems Manager will be responsible for managing a staff of quality system ... Minimum of 5 years of relevant quality engineering experience in the medical device or ...
Quality System Manager
Maple Grove, MN · On-site
The Quality Systems Manager will be responsible for managing a staff of quality system ... Minimum of 5 years of relevant quality engineering experience in the medical device or ...
$102K - $194K/yr
The Quality Systems Manager will be responsible for managing a staff of quality system ... Minimum of 5 years of relevant quality engineering experience in the medical device or ...
$102K - $194K/yr
The Quality Systems Manager will be responsible for managing a staff of quality system ... Minimum of 5 years of relevant quality engineering experience in the medical device or ...
Maintain and recommend improvements to the Quality Management System (QMS) to ensure compliance ... Bachelor's degree in engineering, quality management, or related scientific discipline. American ...
Maintain and recommend improvements to the Quality Management System (QMS) to ensure compliance ... Bachelor's degree in engineering, quality management, or related scientific discipline. American ...
The Quality Systems Manager will be responsible for managing a staff of quality system ... Bachelor's degree Minimum of 5 years of relevant quality engineering experience in the medical ...
The Quality Systems Manager will be responsible for managing a staff of quality system ... Bachelor's degree Minimum of 5 years of relevant quality engineering experience in the medical ...
System Developer
Manhattan, NY · On-site
Participate in code reviews to maintain code quality, identify potential issues, and suggest ... Bachelor's degree in computer science, Software Engineering, Information Systems, Geographic ...
New
System Developer
Manhattan, NY · On-site
Participate in code reviews to maintain code quality, identify potential issues, and suggest ... Bachelor's degree in computer science, Software Engineering, Information Systems, Geographic ...
New
Quality System Manager
Norfolk, VA · On-site
Plan, direct, and coordinate quality assurance administration programs of the company's Quality Management System (QMS), acting as the Management Representative as defined in ISO Standards. With the ...
Quality System Manager
Norfolk, VA · On-site
Plan, direct, and coordinate quality assurance administration programs of the company's Quality Management System (QMS), acting as the Management Representative as defined in ISO Standards. With the ...
Quality System Developer information
See salary details
$12.02 - $17.92
1% of jobs
$17.92 - $23.82
10% of jobs
$23.82 - $29.72
1% of jobs
$29.72 - $35.62
2% of jobs
$35.62 - $41.52
11% of jobs
$41.64 is the 25th percentile. Wages below this are outliers.
$41.52 - $47.42
26% of jobs
$47.42 - $53.32
20% of jobs
$55.53 is the 75th percentile. Wages above this are outliers.
$53.32 - $59.22
13% of jobs
$59.22 - $65.12
6% of jobs
$65.12 - $71.02
4% of jobs
$71.02 - $76.92
6% of jobs
$12
$48
$76
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Quality System Engineer III
Maple Grove, MN • On-site
Full-time
Posted 22 days ago
Boston Scientific rating
8.5
Based on 120 frontline employees who took The Breakroom Quiz
34th of 547 rated manufacturers
Job description
Quality System Engineer III
About the role:
The Quality System Engineer III will serve as a Quality representative to provide support of quality initiatives and goals at a departmental, site, and regional level. This role will support Audit Excellence at Maple Grove, specifically focusing on the Internal Audit program to ensure the compliance and effectiveness of the BSC Quality Management System against external regulations/standards and BSC procedures.
At Boston Scientific, we value collaboration and synergy. This is a hybrid work mode position located in Maple Grove, MN with the expectation to be in the office at least 3 days per week.
Your responsibilities include:
- Execute Internal Audits of the Maple Grove Site as assigned
- Audits may include: Production, Design, Regulatory, Management Controls, and CAPA
- Evaluate and document the compliance of assigned areas via: Tours, Interviews, Documentation and Record Review
- Formulate and document nonconformities and opportunities for improvement
- Understand procedures and evaluate compliance to applicable requirements
- Lead Internal Audits
- Collaborate cross-functionally with Audit Area Management for audit scheduling, execution, and initiation of audit nonconformities
- Develop an Audit Plan, including scope, objectives, criteria, and planned schedule
- Facilitate Audit Opening and Closing Meetings
- Provide work directions to Audit Team
- Complete Audit records, including Audit Report and Audit Trails
- Communicate audit progress and results to Auditees and Leadership
- Support and lead Internal Audit initiatives, continuous improvement opportunities, and/or projects
- Coordinate activities, communicate progress, collaborate on key deliverables, and influence action.
- Make pragmatic, risk-based decisions and provide input regarding how to apply requirements and best practices for processes compliance, efficiency, and effectivity.
- Serve as a Quality System Expert resource as requested
- Support External Audit readiness and execution, including performing production line walks and documentation review.
- Partner cross-functionally to provide guidance on BSC's Quality Management system and external regulations/standards.
Required Qualifications:
- Bachelor's degree
- Minimum of 3 years of relevant quality engineering experience in the medical device or pharmaceutical industry
- Minimum of 1 year experience in a role that includes auditing
- Understanding of regulations/standards applicable to BSC Quality Management (such as 21 CFR 820 and ISO 13485)
- Conceptual, practical, and functional knowledge of quality principles, with a general understanding of related job functions
- Strong verbal and written communication, including technical writing, and organizational skills
- Detail oriented with the ability to analyze information quickly
- Able to use a risk-based approach for making quality and business decisions
Preferred Qualifications:
- 3+ years of experience in audit execution (such as Internal Audits, Supplier Audits, or Regulatory Audits)
- ASQ Certified Quality Auditor
- Proactive, able to work independently with minimal supervision, as a team leader or member
- Ability to collaborate and communicate with all levels of the organization
- Continuous improvement mindset with a passion for Quality
- Proven ability to influence without authority in a matrixed organization
- Strong networking skills to foster collaborative relationships
Requisition ID: 633424
Minimum Salary: $ 78300
Maximum Salary: $ 148800
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 Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
What Boston Scientific employees say
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About Boston Scientific
Sourced by ZipRecruiter
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.
Industry
Medical equipment and supplies manufacturing, manufacturing and construction
Company size
10,000+ Employees
Headquarters location
Marlborough, MA, US