Quality System Manager

Posted 11 Days Ago
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Maple Grove, MN, USA
In-Office
102K-194K Annually
Senior level
Healthtech
The Role
Leads quality systems staff and manages Management Review, Quality Planning, CAPA, and nonconformance processes. Serves as a subject matter expert for QMR and FSR governance, reviews quality documentation, drives continuous improvement and quality strategies, supports audits and inspections, and partners with cross-functional, site, regional, and global stakeholders to improve compliance and standardization.
Summary Generated by Built In

Recruiter: Spencer Gregory Hale


 

Quality System Manager 

 

About the role:

As the Quality Systems Manager supporting Management Control and CAPA processes, you will serve as a People Leader and a key Quality representative responsible for driving effectiveness, compliance, and continuous improvements across the Maple Grove site.

 

The Quality Systems Manager will be responsible for managing a staff of quality system professionals with primary responsibilities for Management Review Meetings, Quality Planning, and the CAPA Process.  They will be the Technical Leader representing the QMR and Quality Planning sub-processes to internal and external stakeholders.  This role will partner closely with the Maple Grove CAPA Technical Lead to execute/improve CAPA and Nonconformance activities.  They will also partner with cross-functional teams, Site Leadership, as well as Regional and Global Quality Systems personnel to execute and drive improvements to Quality Management Review (QMR) and Feeder System Review meetings.

 

Work model, sponsorship, relocation:

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

 

Your responsibilities will include:

  • Lead a team of employees in the achievement of organizational goals; provide guidance to staff, assist them in attaining career goals, and recruit and maintain a high-performing team.
  • Establish, support, and promote a work environment of continuous improvement that supports BSC’s Quality Policy, Core Values, Quality System requirements and appropriate regulations.  
  • Determine appropriate staff levels and schedules; work with key partners to understand priorities and plan resource allocation accordingly.
  • Act as a Subject Matter Expert (SME) for Quality Management Review (QMR), Feeder System Review (FSR), and the Quality Planning sub-process, providing guidance on expectations, requirements, and best practices
  • Partner with Site Leadership to maintain and improve QMR and FSR tools and governance models to provide appropriate visibility to signals and drive robust actions.
  • Partner with the CAPA SME to provide guidance and manage resources of CAPA mentors
  • Review and approve NCEP, CAPA, QMR, FSR, and Quality Planning documentation
  • Develop and implement quality strategies; seek innovative approaches to attaining quality goals.
  • Drive quality projects of moderate scope.
  • Partner with cross-functional stakeholders to drive standardization and adoption of best practices across sites
  • Drive continuous improvement and efficiencies to support a preventive quality culture
  • Support internal and external audits and inspections by providing Management Control and Quality Planning related documentation and subject matter expertise
  • Act as a Quality System resource for external audit readiness, providing guidance and mentoring across site functions regarding quality system compliance. 
  • Maintain and enhance cross-functional team relationships.

 

 

 

Qualifications:

Required qualifications:

  • Bachelor's degree
  • Minimum of 5 years of relevant quality engineering experience in the medical device or pharmaceutical industry
  • Experience with Corrective and Preventive Actions (NCEP, CAPA) and QMR processes
  • Demonstrated leadership ability
  • Conflict management and negotiation skills
  • Solid project management skills
  • Strong interpersonal skills with the ability to communicate and collaborate effectively with cross-functional stakeholders across various levels in the organization
  • Knowledge of regulations/standards such as 21 CFR 820 and ISO 13485

 

Preferred qualifications:

  • Experience supporting audits or regulatory inspections
  • Proactive problem solver with a continuous improvement mindset

 


Requisition ID: 633930 

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 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.  

Skills Required

  • Bachelor's degree
  • Minimum of 5 years of relevant quality engineering experience in the medical device or pharmaceutical industry
  • Experience with Corrective and Preventive Actions, including NCEP and CAPA processes, and QMR processes
  • Demonstrated leadership ability
  • Conflict management and negotiation skills
  • Solid project management skills
  • Strong interpersonal, communication, and cross-functional collaboration skills
  • Knowledge of 21 CFR 820 and ISO 13485 regulations and standards
  • Experience supporting audits or regulatory inspections
  • Proactive problem-solving and continuous improvement mindset

Boston Scientific Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Boston Scientific and has not been reviewed or approved by Boston Scientific.

  • Healthcare Strength Healthcare coverage is positioned as comprehensive, spanning medical, dental, vision, life, and disability insurance alongside mental health resources. Family planning support and broader care navigation offerings further strengthen the health-related value of the package.
  • Retirement Support Retirement benefits stand out through a 401(k) match described as best-in-class and supported by profit sharing and an employee stock purchase plan. High participation in retirement programs is also highlighted as part of the overall financial benefits footprint.
  • Leave & Time Off Breadth Time off is described as generous, with reports of 20+ vacation days and up to four weeks in some roles, plus paid holidays and sick leave. Longer-term options such as extended unpaid family leave and a personal enrichment sabbatical expand flexibility beyond standard PTO.

Boston Scientific Insights

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The Company
HQ: Marlborough, MA
52,374 Employees
Year Founded: 1979

What We Do

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 40 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 health care. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. For more information, visit www.bostonscientific.com and connect with us on X, Instagram, and Facebook. At Boston Scientific, you will find purpose, a place to grow and opportunities to cultivate your passions. To search and apply for open positions, visit https://bostonscientific.eightfold.ai/careers. You may also review our social media guidelines at http://www.bostonscientific.com/social.

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