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Complaint Management Medical Device Jobs (NOW HIRING)

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Complaint Management Medical Device information

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$39K

$68.7K

$97.5K

How much do complaint management medical device jobs pay per year?

As of Aug 19, 2026, the average yearly pay for complaint management medical device in the United States is $68,656.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $69,000.00 per year, depending on experience, location, and employer.

What is complaint management in the medical device industry?

Complaint management in the medical device industry refers to the process of receiving, documenting, investigating, and resolving complaints related to medical devices. This process ensures that any issues or adverse events reported by users, healthcare professionals, or patients are handled in compliance with regulatory requirements. Effective complaint management helps manufacturers identify potential product problems, improve device safety, and maintain regulatory compliance. It also involves reporting certain complaints to regulatory authorities when required, such as the FDA or European Medicines Agency.

What are some common challenges faced in complaint management in the medical device industry?

Professionals in Complaint Management for medical devices often face challenges such as ensuring compliance with complex regulatory requirements, maintaining accurate documentation, and coordinating timely responses to customer complaints. The role requires effective communication with cross-functional teams—including quality assurance, regulatory affairs, and engineering—to investigate and resolve issues. Balancing thorough investigations with prompt reporting is crucial to meeting both patient safety and regulatory obligations. Additionally, staying updated on evolving regulations and industry standards is essential for ongoing success in this position.

What are the key skills and qualifications needed to thrive in complaint management for medical devices, and why are they important?

To thrive in Complaint Management for Medical Devices, you need a solid understanding of regulatory requirements (such as FDA and ISO standards), quality management systems, and product knowledge, often supported by a degree in life sciences or engineering. Familiarity with complaint handling software, CAPA systems, and documentation tools is typically required, along with experience in root cause analysis. Strong attention to detail, effective communication, and problem-solving abilities are crucial soft skills for investigating and resolving complaints. These skills ensure compliance, patient safety, and continuous product improvement in a highly regulated industry.

What is the difference between Complaint Management Medical Device vs Quality Assurance Medical Device?

AspectComplaint Management Medical DeviceQuality Assurance Medical Device
CertificationsISO 13485, Medical Device RegulationsISO 13485, Medical Device Regulations
Work EnvironmentCustomer complaints, post-market surveillanceProduct testing, process audits
Employer & Industry UsageMedical device companies, post-market teamsManufacturers, quality departments

Complaint Management Medical Device professionals focus on handling and investigating customer complaints related to medical devices, ensuring compliance and product safety. In contrast, Quality Assurance Medical Device staff oversee overall product quality, conduct audits, and implement process improvements. While both roles require similar certifications and work within the medical device industry, Complaint Management specialists concentrate on post-market issues, whereas Quality Assurance professionals focus on preventing defects during manufacturing.

More about Complaint Management Medical Device jobs

What cities are hiring for Complaint Management Medical Device jobs?

Cities with the most Complaint Management Medical Device job openings:

What states have the most Complaint Management Medical Device jobs?

States with the most job openings for Complaint Management Medical Device jobs include:

Infographic showing various Complaint Management Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $68,656 per year, or $33 per hour.

Product Complaint Manager

Boston Scientific

Maple Grove, MN • On-site

Full-time

Re-posted 24 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

32nd of 540 rated manufacturers


Job description

Additional Location(s): US-CA-Carlsbad; US-CA-Valencia; US-MN-Arden Hills; US-MN-Maple Grove
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:
Everyone at Boston Scientific works toward one goal: transforming lives by addressing the most critical challenges in the medical device industry. Patient care is at the heart of everything we do, and ensuring quality, compliance and positive outcomes is essential to delivering on that commitment.
Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.
Responsible for leading the Post Market Surveillance team and managing all compliance activities associated with Boston Scientific's complaint handling program in accordance with corporate, domestic and international standards. This role oversees complaint handling processes to ensure compliance with corporate and divisional procedures, FDA regulations, including 21 CFR Parts 820 and 803, and applicable international regulations.
The manager escalates and participates in the resolution of potential product deficiencies, ensures site operational procedures align with corporate policies and regulatory requirements, and serves as the quality liaison for post market surveillance activities, including risk management and complaint handling processes across applicable product portfolios.
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:
• Foster a positive, high-performing team culture by leading through example, promoting high-quality work, effective communication, resilience and solution-oriented thinking.
• Manage employee performance, professional development and career growth through the Performance and Development Conversation (PDC) process and Boston Scientific HR policies.
• Oversee daily work operations to achieve company, divisional and project objectives by providing direction, coaching and support while empowering employees to perform at their best.
• Maintain processes and procedures that ensure compliance with corporate policies, external regulations and applicable quality standards.
• Ensure compliance with U.S. and international medical device regulatory requirements related to complaint handling and regulatory reporting.
• Lead highly impactful cross-functional initiatives within the Global Quality Community to improve post market quality across multiple divisions.
• Coordinate multiple projects, priorities and stakeholder meetings across sites and functions to achieve project deliverables and timelines.
• Prepare and deliver clear, concise communications and project updates to senior leadership regarding deliverables, milestones and timelines.
• Influence change, build alignment and facilitate decision-making in situations involving ambiguity or limited information.
• Build effective relationships with internal and external stakeholders by responding to requests, providing guidance and explaining processes and procedures.
• Coordinate and participate in the escalation and resolution of adverse complaint trends and potential product issues.
• Ensure Post Market Surveillance employees receive appropriate onboarding, compliance and ongoing training.
• Assess staffing needs and recommend resources necessary to achieve business objectives and maintain regulatory compliance.
• Oversee the accuracy, completeness and maintenance of complaint records within the Global Complaint Management Database.
• Monitor internal and external quality indicators by reviewing reports, industry publications, regulatory updates and organizational communications to identify opportunities for continuous improvement.
Qualifications:
Required qualifications:
• Bachelor's degree.
• Minimum of 7 years' experience in the medical device industry.
• Demonstrated ability to adapt to changing priorities while contributing effectively in a dynamic environment.
Preferred qualifications:
• Boston Scientific experience.
• Knowledge of U.S. and international regulatory reporting requirements.
• Experience working with competent authorities.
• Strong people leadership, communication and organizational skills.
• Project management experience.
• Demonstrated experience leading high-performing teams.
• Experience supporting Neuromodulation products.
• Experience with post market surveillance activities.
• Vendor management experience.
Requisition ID: 630947
Minimum Salary: $ 106800
Maximum Salary: $ 202900
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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