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🔥 1 hour ago
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PV Officer processing ICSR safety cases for PrimeVigilance, a global pharmacovigilance specialist. Managing quality controls, KPIs, deviations and local pharmacovigilance responsibilities in Croatia.
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🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-checking safety cases for PrimeVigilance, a global pharmacovigilance specialist. Supporting project KPIs, process improvements, and local pharmacovigilance responsibilities.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-checking safety cases for PrimeVigilance, a global pharmacovigilance specialist. Supporting KPIs, deviations, regulatory activities and local pharmacovigilance responsibilities.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer supporting ICSR processing, quality control, and project KPIs at PrimeVigilance, a global pharmacovigilance specialist. Helping clients manage safety regulations and protect patients through post-marketing surveillance.
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🔥 1 hour ago
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PV Officer processing and quality-controlling safety cases for PrimeVigilance, a global pharmacovigilance specialist. Supporting KPIs, deviations, process improvements, and local pharmacovigilance responsibilities.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-controlling safety cases for PrimeVigilance, a global pharmacovigilance specialist. Supporting ICSR efficiency, regulatory affairs, and patient safety operations.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-controlling safety cases for PrimeVigilance, a global pharmacovigilance specialist. Supporting KPIs, deviations, regulatory affairs, and local pharmacovigilance responsibilities.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-checking individual case safety reports for PrimeVigilance, a global pharmacovigilance specialist. Supporting regulatory and patient-safety activities across client projects.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-controlling pharmacovigilance cases for PrimeVigilance, a global patient-safety specialist. Managing ICSR KPIs, deviations, process improvements, and local pharmacovigilance responsibilities.
Job not on LinkedIn
🔥 1 hour ago
Job not on LinkedIn
PV Officer processing and quality-controlling safety cases for PrimeVigilance, a global pharmacovigilance specialist. Supporting client projects, KPIs, process improvements and local pharmacovigilance responsibilities.
🕒 2 days ago
Technical Specialist managing IVD medical-device CE marking schemes for BSI, a standards and business-improvement company. Reviewing technical compliance, assessing QMS, and mentoring healthcare personnel across EMEA.
🌐 United Kingdom, Spain, +3 more countries – Remote
💵 £63.4k - £74.5k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
✨ Medical Device
🇬🇧 UK Skilled Worker Visa Sponsor
Job not on LinkedIn
🕒 2 days ago
Job not on LinkedIn
Clinical Specialist supporting Abbott’s structural heart medical devices and TAVI procedures in Guadalajara, Mexico. Providing cathlab case support, CT valve sizing, customer training, and clinical education.
🗣️🇪🇸 Spanish Required
Job not on LinkedIn
🕒 3 days ago
Job not on LinkedIn
Senior CRA monitoring cardiac and medical-device clinical trials for Fortrea. Managing sites, regulatory compliance, safety reporting, and clinical data quality across remote U.S. locations.
🏄 California, Iowa, +2 more states – Remote
💵 $130k - $133k / year
⏰ Full Time
🟠 Senior
✨ Medical Device
🕒 3 days ago
IVD medical-device specialist managing CE marking schemes for BSI, a global business improvement and standards company. Providing technical reviews, QMS assessment, and expertise for infectious-disease diagnostics.
Job not on LinkedIn
🕒 3 days ago
Job not on LinkedIn
Pharmacovigilance team lead managing medical-device safety cases for PrimeVigilance, a global patient-safety specialist. Leading ICSR teams, workflows, KPIs, quality control, and client collaboration.
Job not on LinkedIn
🕒 3 days ago
Job not on LinkedIn
Pharmacovigilance team lead managing medical-device safety cases for global pharmaceutical clients. Overseeing ICSR teams, workflows, quality control, KPIs, and client collaboration.
🕒 3 days ago
Job not on LinkedIn
PrimeVigilance team lead managing ICSR pharmacovigilance cases and medical-device safety projects. Leading staff, workflows, KPIs, quality control, and client collaboration.
🕒 3 days ago
Job not on LinkedIn
Pharmacovigilance team lead managing ICSR case processing and safety operations for PrimeVigilance, a global drug-safety specialist. Leading staff, client cooperation, KPIs and quality control for medical-device projects.
🕒 3 days ago
Job not on LinkedIn
Pharmacovigilance team lead managing ICSR case processing and safety-data quality for PrimeVigilance. Leading staff, workflows, KPIs, client cooperation, and medical-device safety activities.
🕒 3 days ago
Job not on LinkedIn
Pharmacovigilance team lead managing ICSR case processing and quality control for PrimeVigilance’s pharmaceutical and medical-device clients. Supporting global regulatory and patient-safety operations.
+96 More Medical Device Jobs Available!
The average salary for remote medical devices is $123,334 per year. This is based on data from 319 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
🟢 Junior Medical Device (1-2 yrs) | 46 | $78,219 |
🟡 Mid-level Medical Device (2-4 yrs) | 144 | $110,611 |
🟠 Senior Medical Device (5-9 yrs) | 111 | $146,108 |
🔴 Lead Medical Device (10+ yrs) | 18 | $199,970 |
We analyzed 215 job listings in the last year and found it takes about 51 days for employers to close a job opening.
We reviewed 319 job postings and found the top 10 skills employers are asking for most often are:
You need strong knowledge of medical device regulations and standards, proficiency in project management, ability to analyze and interpret technical data, and strong communication skills. Familiarity with design controls and quality assurance is also important.
Typically, a degree in biomedical engineering, mechanical engineering, or a related field is required. Relevant certifications in medical device standards and a background in quality management systems can enhance your qualifications.
Responsibilities include managing the development and testing of medical devices, ensuring compliance with regulatory standards, collaborating with engineering teams, conducting risk assessments, and preparing documentation for regulatory submissions.
Benefits include flexible work arrangements, reduced commuting time and costs, access to a diverse range of projects, and the opportunity to contribute to impactful healthcare solutions. Remote work also supports better work-life balance.
We scan the internet everyday and find jobs not posted on LinkedIn or other job boards.
We find jobs as soon as they're posted, so you can apply before everyone else.
Most members hear back within the first week
We find jobs other job boards miss.
