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Capa Manager Jobs in Minnesota (NOW HIRING)

Quality Engineer

Big Lake, MN · On-site

$80K - $100K/yr

Manage NCR, CAPA, and customer complaints from creation to closure. * Use problem-solving tools and work as part of a cross-functional team. * Change Management: * Lead changes in production ...

The Quality Manager provides leadership and functional ownership of the Quality Management System ... This is a hands-on role requiring direct involvementin CAPA execution, complaint resolution, audit ...

Quality Manager

Blaine, MN · On-site

$90K - $130K/yr

The Quality Manager provides leadership and functional ownership of the Quality Management System ... This is a hands-on role requiring direct involvement in CAPA execution, complaint resolution, audit ...

Director of Quality

Eden Prairie, MN · On-site

$155K - $170K/yr

Oversees CAPA, nonconforming materials, complaint handling, document control, change control, supplier quality system processes, and internal audits. * Ensures risk management processes are ...

CAPA, NCMR, Change and Document Control, Complaints, Training, and Audits * Establish alignment and ... Directly manage the account relationships between Nextern and it's notified bodies * Performs other ...

Quality Systems Manager

Maple Grove, MN · On-site

$120K - $140K/yr

CAPA, NCMR, Change and Document Control, Complaints, Training, and Audits * Establish alignment and ... Directly manage the account relationships between Nextern and it's notified bodies * Performs other ...

Quality Systems Manager

Osseo, MN · On-site

$120K - $140K/yr

CAPA, NCMR, Change and Document Control, Complaints, Training, and Audits * Establish alignment and ... Directly manage the account relationships between Nextern and it's notified bodies * Performs other ...

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Capa Manager information

See Minnesota salary details

$13

$39

$56

How much do capa manager jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for capa manager in Minnesota is $39.05, according to ZipRecruiter salary data. Most workers in this role earn between $29.66 and $46.01 per hour, depending on experience, location, and employer.

What does a CAPA Manager do?

A CAPA (Corrective and Preventive Action) Manager is responsible for overseeing an organization's CAPA process to ensure compliance with quality and regulatory requirements. They investigate quality issues, identify root causes, and implement corrective and preventive measures to prevent recurrence. CAPA Managers work closely with cross-functional teams to improve processes, maintain regulatory compliance, and enhance overall product or service quality.

What are some common challenges a CAPA Manager faces, and how are they typically addressed?

One common challenge CAPA Managers face is ensuring timely and thorough investigations into quality issues while coordinating input from multiple departments. Balancing the need for fast resolution with the rigor required for regulatory compliance can be demanding, especially in highly regulated industries like pharmaceuticals or medical devices. Successful CAPA Managers often address these challenges through clear process documentation, effective project management, and fostering strong collaboration among stakeholders. By leveraging root cause analysis tools and maintaining open communication, they help create a continuous improvement culture that benefits both the organization and its customers.

What is a CAPA manager?

A CAPA manager oversees the Corrective and Preventive Actions process within an organization to identify, investigate, and resolve quality issues or non-conformities. They ensure compliance with regulatory standards, often using quality management tools, and coordinate cross-functional teams to implement effective solutions.

What are the key skills and qualifications needed to thrive in the Capa Manager position, and why are they important?

To thrive as a CAPA Manager (Corrective and Preventive Action Manager), you typically need a background in quality assurance, strong analytical and problem-solving abilities, and experience with regulatory compliance, often supported by a degree in a science or engineering field. Familiarity with quality management systems (QMS), risk management tools, root cause analysis methodologies (such as 5 Whys or Fishbone diagrams), and industry certifications like Six Sigma or ISO 9001 are highly valued. Outstanding candidates demonstrate excellent communication, leadership, and organizational skills to effectively drive cross-functional teams and ensure timely resolution of quality issues. These skills are crucial for identifying, addressing, and preventing compliance gaps or product issues, thereby maintaining high standards and avoiding costly regulatory penalties.

What job makes $10,000 a month without a degree?

A Capa Manager, or Corrective and Preventive Action Manager, can earn around $10,000 monthly by overseeing quality management systems in manufacturing or healthcare environments. Success in this role depends on experience, industry knowledge, and strong organizational skills, often without requiring a formal degree but emphasizing certifications and practical expertise.
What are popular job titles related to Capa Manager jobs in Minnesota? For Capa Manager jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Capa Manager jobs in Minnesota look for? The top searched job categories for Capa Manager jobs in Minnesota are:
What cities in Minnesota are hiring for Capa Manager jobs? Cities in Minnesota with the most Capa Manager job openings:
Design Assurance CAPA Manager - Cardiac Rhythm Management and Diagnostics (CRMDx)

Design Assurance CAPA Manager - Cardiac Rhythm Management and Diagnostics (CRMDx)

Boston Scientific

Arden Hills, MN • On-site

Full-time

Posted 6 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 119 frontline employees who took The Breakroom Quiz

33rd of 516 rated manufacturers


Job description

Additional Location(s): N/A
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 This Role:
This Manager of the Arden Hills based Cardiac Rhythm Management and Diagnostics (CRMDx) Field CAPA team will lead a team of 4-5 direct individuals and a number of cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues impacting Active Implantables, Medical Electrical Equipment (MEE) & Accessories product performance within the CRMDx division. This role is a tremendous opportunity for a strong technical leader, with an innate technical curiosity, who is seeking leadership, complex problem-solving, project management experience, and making a direct impact on the lifesaving and life-enhancing technologies in CRMDx and Active Implantables. The role also provides great exposure to the intricacies of how the entire portfolio of CRMDx products function, are designed, and the many parts of the organization that support their commercial use. This individual will collaborate and partner with Research & Development, Regulatory, Marketing, Medical Safety, Manufacturing, Post Market, and other Quality organizations to achieve optimal results. Will also serve as liaison between the company and the various governmental agencies worldwide.
Work mode:
At Boston Scientific, we value collaboration and synergy. This hybrid role is based in Arden Hills, MN.
Relocation assistance:
Relocation assistance is not available for this position at this time.
Visa sponsorship:
Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.
Your Responsibilities Will Include:
  • Leads a team of employees in the achievement of organizational goals, project goals, and career goals. Recruits, hires, supports, and develops a high performing team.
  • Leads cross-functional teams on complex product performance investigations, where suspected root cause is product design. Includes Nonconforming Events and Preventions (NCEPs), Product Inquiry Reports (PIRs), and Corrective and Preventive Actions (CAPAs). Expected to facilitate high performing teams working towards common goals and timelines.
  • Reviews, approves, and creates Quality System records for NCEPs, PIRs, and CAPAs. Would represent NCEPs, PIRs, and CAPAs in internal and external audits directly or with team.
  • Creates, maintains, and enhances cross-functional team partnerships. Provides guidance regarding technical strategies and approaches; works cross-functionally and across multiple sites in identifying and resolving technical issues. Represents the team at key global and divisional leadership forums.
  • Develops department budget and monitors spending. Determines appropriate staff levels and schedules. Works with cross-functional partners to understand priorities and plans resource allocation accordingly.
  • Leads collaborative problem solving of complex technical issues using disciplined, methodical techniques. Tools used include DMAIC, Root Cause Analysis, 5 Whys, Cause & Effect Diagram, and Is-Is Not.
  • Presents updates in formal and informal reviews with all levels of the organization including high senior leadership at Boston Scientific.
  • Mentors and guides other cross-functional teams and engineers by providing technical guidance and consulting on execution of NCEPs, CAPAs, and PIRs. May include consulting across other BSC divisions.
  • Drive improvement in Field CAPA team directly and at large in Global Communities of Practice to foster cross-communication, best practices, and improvement to investigational processes and outcomes.
  • Focuses on continuous improvement by championing and fostering the execution of projects within the local and divisional Design Assurance organizations.
  • Fosters a diverse and inclusive workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
  • Monitors and ensures compliance with company policies and procedures.
  • Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

What We're Looking For In You:
Required Qualifications
  • Bachelor's degree in an engineering or related discipline with 8+ years of relevant experience
  • Minimum of 2 years of direct supervisory experience with a passion for leadership and team development
  • Knowledgeable in Quality System Regulations, Medical Device Regulation, and ISO 13485 Quality Standards.
  • Experience in Medical Device industry

Preferred Qualifications
  • Experience with NCEPs, CAPAs, PIRs and other investigation processes.
  • Experience with Active Implantables and the CRMDx division, especially at system level
  • Demonstrated technical problem-solving & data analysis capabilities
  • Experience with statistics and statistical analysis tools (e.g. MINITAB, Weibull++)
  • Strong ability to successfully multi-task and demonstrate adaptability
  • Project management experience (direct or cross-functional teams)
  • Demonstrated effective change leadership and results-oriented focus
  • Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook.
  • Strong business acumen and communication skills, with the ability to quickly establish impact and consequences
  • Ability to collaborate and influence across multiple, cross-functional teams
  • Demonstrated experience managing and leading multiple technical projects covering diverse engineering (i.e. Software, Hardware, Labeling) disciplines and functions.
  • Self-starter with the ability to identify improvement opportunities.
  • Comfort speaking to groups of individuals including divisional senior leaders. Presentation skills that comfortably and concisely translate performance and issues to peer and senior management audiences.

Requisition ID: 628437
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 www.bostonscientific.com and follow us on LinkedIn.
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.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.
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.

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