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Manager, Post-Market Quality
Redwood City, California, United States
OnsiteFull Time
5+ YOE2+ MgmtLead post-market quality processes including intake, investigation, regulatory reportability, and closure; drive post-market data analysis for management and cross-functional stakeholders.
1mo
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Post Market Surveillance Coordinator
New York or United States
$87k-$178k/yr RemoteFull Time
6+ YOE6+ years in quality systems, post-market signaling, regulatory reporting; lead process development; strong communication and problem-solving skills.
Regulatory Submissions, Regulatory Reporting, Risk Management, Quality Management, Post-Market Surveillance, Regulatory Audits, Regulatory Oversight, Technical Communication
1w
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Engineer, Post Market Quality
Portage, Michigan, United States
$70k-$111k/yr HybridFull Time
Bachelor's degree in an engineering discipline required. Experience in quality engineering, post-market quality, CAPA, audits, risk management, root cause analysis, and statistical data analysis preferred.
3w
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Post Market Surveillance Manager
Bothell or Cambridge or San Diego or Plymouth or Reedsville
$120k-$186k/yr HybridFull Time
5+ YOE5+ Mgmt5+ years in post-market surveillance/medical device quality or related area, leadership experience, degree in engineering or science, knowledge of regulatory compliance, complaint investigation, QA, training, and process improvement.
1mo
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Post Market Quality Engineer
Warsaw, Indiana, United States
OnsiteFull Time
Conduct post-market complaint investigations, failure and root-cause analyses, risk assessments, and documentation; strong knowledge of 21 CFR 820, ISO 13485, ISO 14971; bachelor’s in engineering or equivalent; ISO 13485 audit and ASQ preferred.
Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft PowerPoint, SPC, GD&T
1w
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Sr Manager Post Market Surveillance
Libertyville, Illinois, United States
$140k-$185k/yr HybridFull Time
12+ YOEBachelor’s degree and 12–15 years related experience; deep experience in post-market surveillance, complaint handling, vigilance and regulatory reporting; people leadership, analytics, and cross-functional collaboration skills.
2mo
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Director of Post Market Products
Manchester, New Hampshire, United States
OnsiteFull Time
10+ YOE5+ Mgmt10+ years in medical devices post-market, with 5+ years in leadership; strong regulatory and QA knowledge.
Salesforce, MasterControl, TrackWise
2d
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Senior Post-Market Surveillance Engineer
Burnsville, Minnesota, United States
$110k-$132k/yr OnsiteFull Time
5+ YOEBachelor's in engineering, 5+ years post-market quality experience in FDA/EU MDR/ISO 13485 environments; complaint investigations, CAPA, risk management (ISO 14971), statistical trending, and strong communication skills.
1w
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Senior Director, Post Market Monitoring
Westborough, Massachusetts, United States
$145k-$217k/yr RemoteFull Time
12+ YOE7+ MgmtBachelor's in engineering/life sciences/data plus 12+ years in medical device quality/post-market surveillance, 7+ years people leadership, regulatory experience (FDA, EU MDR), analytics/AI implementation, PSUR/PMS deliverables, and up to 20% travel.
machine learning, artificial intelligence, AI, business intelligence
2mo
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Post Market Surveillance Engineer II
Plymouth or Chaska
OnsiteFull Time
1+ YOEBachelor’s degree and 1+ year relevant experience in post-market surveillance or regulated medical devices; strong knowledge of FDA 21 CFR; ability to collaborate cross-functionally.
Microsoft Excel, Microsoft PowerPoint, Microsoft Visio, Microsoft Project
1mo
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Director Post Market Compliance
Marlborough or Newark
$171k-$304k/yr OnsiteFull Time
10+ YOEBachelor's or equivalent experience, 10+ years in medical device quality assurance, experience managing complaints/vigilance/field actions, FDA cGMP audit experience, leadership and data analysis skills.
2mo
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Manager Post Market Surveillance
San Diego, California, United States
$125k-$145k/yr OnsiteFull Time
8+ YOEBachelor's degree; 8+ years in medical device/biotech; 4+ years in technical support and complaint vigilance; regulatory knowledge; leadership; strong analytics.
Electronic Quality Management System
3mo
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Manager, Post Market Surveillance- Recall
Livingston or Trumbull
$107k-$150k/yr OnsiteFull Time
4+ YOELead recalls from initiation to closure with FDA/ISO knowledge; 4+ years recall leadership; strong communication; bachelor’s in related field.
eQMS, Quality Management Systems, Regulatory documentation
1mo
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Senior Manager, Global Post Market Quality Systems
Arden Hills or Marlborough
$126k-$239k/yr HybridFull Time
7+ YOE3+ MgmtBachelor's degree, 7+ years medical device experience, 3+ years leadership, 3+ years post-market quality/design assurance, knowledge of global regulatory requirements (ISO 13485, MDD/MDR, FDA QMSR, Health Canada, ANVISA, TGA, NMPA), experience with external regulatory bodies.
1mo
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Senior Manager, Global Post Market Quality Systems
Arden Hills or Marlborough
$126k-$239k/yr HybridFull Time
7+ YOE3+ MgmtBachelor's degree, 7+ years in the medical device industry, 3+ years leadership and 3+ years in post-market quality or design assurance; experience with ISO 13485, MDD/MDR, FDA QMSR and international regulatory requirements; stakeholder engagement and program leadership skills.
4w
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Manager, Complaints and Post-Market
San Jose, California, United States
$141k-$177k/yr HybridFull Time
5+ YOEBS in a technical field (or equivalent experience), 5+ years complaint-handling experience (3+ years in device industry preferred), knowledge of complaint lifecycle, adverse event reporting, CAPA, ISO 13485 and US FDA 21 CFR requirements, auditing and team management skills.
1mo
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Manager, Clinical Post Market Surveillance
Burlington, Massachusetts, United States
$99k-$199k/yr OnsiteFull Time
3+ MgmtBachelor's in biomedical engineering, nursing or related (or equivalent experience); minimum 3 years managing a team; knowledge of domestic/international medical device regulations, complaint handling, CAPA, MDRs, audit readiness, and strong PC and leadership skills.
2w
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Secondary Market Post-Closing Specialist
Mobile, Alabama, United States
OnsiteFull Time
2+ YOEMinimum 2 years related experience, high school diploma or equivalent, knowledge of real estate lending and compliance, proficiency with Microsoft Word/Excel/Outlook, strong attention to detail and customer service.
Microsoft Word, Microsoft Excel, Microsoft Outlook
1mo
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Manager, Clinical Post Market Surveillance
Burlington, Massachusetts, United States
$99k-$199k/yr OnsiteFull Time
3+ MgmtBachelor's in biomedical engineering, nursing or related (or equivalent experience). 3+ years managing a team. Knowledge of domestic/international medical device regulations, risk assessment, CAPA and audit management, and advanced analytical and PC skills.
Quality Management System, CAPA System, External Requirements Management System, spreadsheets, word processing, database management, project management applications
1mo
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Post Market Surveillance SME - Medical Device #6887
Marlborough, Massachusetts, United States
OnsiteFull Time, Contract
5+ YOEBachelor's in engineering/life sciences/quality/regulatory required, 5+ years in medical device quality/regulatory/clinical/post-market surveillance, strong knowledge of FDA, EU MDR, ISO 13485/14971, complaint/CAPA/risk management, analytical and technical writing skills. Must be authorized to work in the U.S. without sponsorship.
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