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Entry Level Post Market Surveillance Medical Device Jobs

Quality

Complaints Engineer II - TA

Sunrise, FL · Hybrid

... Medical Device Reporting, and vigilance reporting; collaborate on reportability decisions and timely report generation. Serve as the Post-Market Surveillance subject-matter expert for assigned ...

Apex Systems

Post Market Analyst

Burlingame, CA · On-site

$35 - $40/hr

This role will focus on post-market surveillance (PMS), complaint investigations, and customer ... Experience supporting consumer electronics, medical devices, wearables, or technology products ...

Hologic, Inc.

WI · On-site

$125 - $150/hr

... medical device quality, compliance, and safety throughout the product lifecycle, from product ... investigation, and post-market surveillance. * Product and design requirements, ensuring ...

Exactech

QA PM Specialist

Gainesville, FL · On-site

Minimum of 1 year of experience performing a complaint handling or post market surveillance role in a Medical Device or Pharmaceutical FDA regulated environment. * In lieu of previous complaint ...

Podimetrics Inc.

$60 - $80/hr

Support Quality Engineering with post-market surveillance activities, including trending device ... Minimum of 2 years of experience in the medical device industry, with familiarity with FDA 21 CFR ...

Podimetrics

Quality Associate

Somerville, MA · On-site

Support Quality Engineering with post-market surveillance activities, including trending device ... Minimum of 2 years of experience in the medical device industry, with familiarity with FDA 21 CFR ...

Podimetrics

Quality Associate

Somerville, MA

Support Quality Engineering with post-market surveillance activities, including trending device ... Minimum of 2 years of experience in the medical device industry, with familiarity with FDA 21 CFR ...

Hologic, Inc.

WI · On-site

$100 - $125/hr

... investigation, and post-market surveillance. * Product and design requirements, ensuring ... Prior experience in medical device or other highly regulated industry * Experienced with FDA ...

Irhythmtech

Quality Specialist - Post Market

$74K - $93K/yr

... medical device regulations particularly as they relate to complaint handling, vigilance, reporting timelines, and post-market surveillance Strong written and verbal communication skills Location:

Terumo Corporation

Complaints Engineer II

Elkton, MD

$69K - $90K/yr

Act as Post Market Surveillance Subject Matter Expert for assigned product lines which includes ... in a medical device quality assurance or clinical environment, or equal vent combination of ...

Terumo Corporation

Complaints Engineer II

Elkton, MD · On-site

$69K - $90K/yr

Act as Post Market Surveillance Subject Matter Expert for assigned product lines which includes ... in a medical device quality assurance or clinical environment, or equal vent combination of ...

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All Jobsmedical device JobsEntry Level Post Market Surveillance Medical Device Jobs

Entry Level Post Market Surveillance Medical Device information

See salary details

$30.5K

$47.7K

$61K

How much do entry level post market surveillance medical device jobs pay per year?

As of Sep 7, 2026, the average yearly pay for entry level post market surveillance medical device in the United States is $47,730.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $52,500.00 per year, depending on experience, location, and employer.

What is the difference between Entry Level Post Market Surveillance Medical Device vs Entry Level Quality Assurance Medical Device?

AspectEntry Level Post Market Surveillance Medical DeviceEntry Level Quality Assurance Medical Device
CertificationsTypically requires knowledge of FDA regulations, ISO standards, and basic surveillance toolsRequires understanding of quality standards, audit procedures, and compliance regulations
Work EnvironmentMonitoring device performance, analyzing post-market data, collaborating with regulatory teamsConducting audits, reviewing manufacturing processes, ensuring product quality
Industry UsageUsed in medical device companies focusing on post-market activities and regulatory complianceUsed in quality departments to maintain product standards and compliance

While both roles involve regulatory knowledge and work within the medical device industry, the Post Market Surveillance role focuses on monitoring device performance after market release, whereas Quality Assurance emphasizes preventing issues through process audits and quality checks.

What cities are hiring for Entry Level Post Market Surveillance Medical Device jobs?

Cities with the most Entry Level Post Market Surveillance Medical Device job openings:

What are the most commonly searched types of Post Market Surveillance Medical Device jobs?

The most popular types of Post Market Surveillance Medical Device jobs are:

What states have the most Entry Level Post Market Surveillance Medical Device jobs?

States with the most job openings for Entry Level Post Market Surveillance Medical Device jobs include:

Entry Level Post Market Surveillance Medical Device jobs near you
Infographic showing various Entry Level Post Market Surveillance Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $47,730 per year, or $22.9 per hour.

Complaints Engineer II - TA

Terumo Corporation

Sunrise, FL • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Job description

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to find the right fit for each patient anatomy.

The company has over 1,250 associates around the world with manufacturing facilities in Glasgow, Scotland and Sunrise, Florida.

Terumo Aortic is focused on the continuing development of new and innovative products driving the growth of the business globally. Associates are part of a stimulating and exciting environment in which they can develop their skills and achieve career goals. Working for the company, each associate's role contributes greatly to helping to save or improve the lives of patients in over 100 countries worldwide.

At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.

Join us and help shape wherever we go next!

Advancing healthcare with heart

www.terumoaortic.com

Job Summary

Analyzes, evaluates, and investigates external customer complaints in accordance with FDA, ISO, Quality System, EU MDR, and other applicable regulatory requirements. Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint processes, procedures, and team capability.

Job Details/Responsibilities

Drive timely, accurate, and complete complaint and failure investigations with cross-functional teams; perform retention, decontamination, objective testing, returned-product analysis, simulation, root-cause investigation, and resolution in support of product quality and patient safety.

Ensure compliance with applicable US and international complaint and adverse-event regulations, including FDA, Canadian requirements, EU MDR, Medical Device Reporting, and vigilance reporting; collaborate on reportability decisions and timely report generation.

Serve as the Post-Market Surveillance subject-matter expert for assigned product lines, maintaining knowledge of product design, manufacturing, complaint rates and trends, reportability, risks, and failure modes.

Collect complaint follow-up information from customers, medical professionals, field staff, Sales, Field Service, affiliates, and other stakeholders; investigate field clinical events, coordinate clinical-sample investigations, and prepare customer and field responses.

Analyze and trend complaint data, convene trending meetings, present engineering failure analyses and critical information, document minutes, follow action items to closure, compile PSURs, and prepare management metrics and reports.

Maintain complaint-handling procedures, support team and organizational performance indicators, provide assistance and training to team members, stay current with required training, and promote continuous improvement of complaint and post-market processes.

Provide engineering expertise for complaint-investigation test equipment, including feasibility, installation, validation, qualification, layout, procurement, documentation, user training; support schedules, expenditures, and monthly reports.

Job Responsibilities (continued)
Working Conditions/Physical Requirements
Knowledge, Skills and Abilities (KSA)
  • Thorough knowledge of medical-device standards and regulations, complaint handling, Medical Device Reporting, vigilance reporting, and applicable recordkeeping requirements.
  • Strong analytical and problem-solving skills and knowledge of laboratory procedures used to evaluate returned samples and investigate product failures.
  • Excellent written and oral English communication and technical-writing skills, with strong presentation and training capability.
  • Ability to interact effectively with individuals and groups at all organizational levels and with customers, medical professionals, field personnel, and affiliates.
  • Ability to manage multiple priorities independently with accuracy, sound judgment, and close attention to detail.
  • Proficiency with Microsoft Word, PowerPoint, and Excel; Minitab proficiency is preferred.
  • Knowledge of complaint metrics, data analysis and trending, report preparation, investigation equipment, and validation and qualification documentation.
Qualifications/ Background Experiences
  • Bachelor's degree in Engineering, Life Sciences, or a related technical field, or equivalent education and experience.
  • At least three years of experience in medical-device quality assurance or a clinical environment.
  • At least four years of quality, complaint-investigation and resolution, or clinical experience in the disposable medical-device industry.
  • Clinical experience or in-depth knowledge of interventional products and medical procedures is strongly preferred.
  • ASQ certification (CQE or CQIA) is desirable.

It is Terumo's policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. 

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