Must have experience working with medical device registrations compliant with Medical Device Regulation and EU Medical Device Directive. Hybrid role model position, working 3 days in office and 2 ...
Must have experience working with medical device registrations compliant with Medical Device Regulation and EU Medical Device Directive. Hybrid role model position, working 3 days in office and 2 ...
We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across ...
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We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across ...
Regulatory Affairs Specialist
Raleigh, NC · On-site
Knowledge of medical device regulations and governing laws such as 21 CFR 814, 21 CFR 814, 21 CFR 820. * Strong analytical, investigative, and organizational skills. Demonstrate curiosity preferred.
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Regulatory Affairs Specialist
Raleigh, NC · On-site
Knowledge of medical device regulations and governing laws such as 21 CFR 814, 21 CFR 814, 21 CFR 820. * Strong analytical, investigative, and organizational skills. Demonstrate curiosity preferred.
... for medical device quality. • Provide electrical and firmware engineering support ensuring current and new products meet Medical Device safety requirements such as IEC 60601 and other Medical ...
... for medical device quality. • Provide electrical and firmware engineering support ensuring current and new products meet Medical Device safety requirements such as IEC 60601 and other Medical ...
Quality activities for medical device manufacturing and Design & * Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control ...
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Quality activities for medical device manufacturing and Design & * Development activities throughout all stages of the device development process (e.g. general Product Development / Design Control ...
Health System Manager Associate-University (Raliegh)
Raleigh, NC · On-site
$85K/yr
Applied Medical is a new generation medical device company with a proven business model and commitment to innovation that has fueled our rapid business growth and expansion. Applied has recently ...
Health System Manager Associate-University (Raliegh)
Raleigh, NC · On-site
$85K/yr
Applied Medical is a new generation medical device company with a proven business model and commitment to innovation that has fueled our rapid business growth and expansion. Applied has recently ...
Electro-Mechanical Lab Technician
Raleigh, NC · On-site
$25 - $40/hr
The ideal candidate will have a background in medical device assembly, electronics assembly, and experience with Good Documentation Practices (GDP) and Good Laboratory Practices (GLP). * This role ...
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Electro-Mechanical Lab Technician
Raleigh, NC · On-site
$25 - $40/hr
The ideal candidate will have a background in medical device assembly, electronics assembly, and experience with Good Documentation Practices (GDP) and Good Laboratory Practices (GLP). * This role ...
Sales Support/Logistics Coordinator
Morrisville, NC · Hybrid
$19.25 - $26/hr
Accentuate Staffing is currently recruiting for a Sales Support/Logistics Coordinator for global medical device company in Morrisville. This position will be hybrid once the employee is fully trained.
Sales Support/Logistics Coordinator
Morrisville, NC · Hybrid
$19.25 - $26/hr
Accentuate Staffing is currently recruiting for a Sales Support/Logistics Coordinator for global medical device company in Morrisville. This position will be hybrid once the employee is fully trained.
Principal Electrical Engineer
Morrisville, NC · On-site
$130K - $159K/yr
Demonstrated ability to independently lead and deliver complex medical device hardware development projects from concept through design verification and validation. * Deep hands-on expertise with ...
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Principal Electrical Engineer
Morrisville, NC · On-site
$130K - $159K/yr
Demonstrated ability to independently lead and deliver complex medical device hardware development projects from concept through design verification and validation. * Deep hands-on expertise with ...
senior software engineer
Durham, NC · On-site
$118K - $156K/yr
Position Summary This position comprises hands- on software design, implementation, and verification of medical device software and infrastructure across multiple software technologies. The ...
senior software engineer
Durham, NC · On-site
$118K - $156K/yr
Position Summary This position comprises hands- on software design, implementation, and verification of medical device software and infrastructure across multiple software technologies. The ...
Principal Electrical Engineer
$130K - $159K/yr
Demonstrated ability to independently lead and deliver complex medical device hardware development projects from concept through design verification and validation. * Deep hands-on expertise with ...
Principal Electrical Engineer
$130K - $159K/yr
Demonstrated ability to independently lead and deliver complex medical device hardware development projects from concept through design verification and validation. * Deep hands-on expertise with ...
senior software engineer
Durham, NC · On-site
$118K - $156K/yr
Position Summary This position comprises hands- on software design, implementation, and verification of medical device software and infrastructure across multiple software technologies. The ...
senior software engineer
Durham, NC · On-site
$118K - $156K/yr
Position Summary This position comprises hands- on software design, implementation, and verification of medical device software and infrastructure across multiple software technologies. The ...
Principal Electrical Engineer
Morrisville, NC · On-site
$130K - $159K/yr
Demonstrated ability to independently lead and deliver complex medical device hardware development projects from concept through design verification and validation. * Deep hands-on expertise with ...
Principal Electrical Engineer
Morrisville, NC · On-site
$130K - $159K/yr
Demonstrated ability to independently lead and deliver complex medical device hardware development projects from concept through design verification and validation. * Deep hands-on expertise with ...
Regional Sales Manager-East
Raleigh, NC · On-site
Bachelor's Degree in related field * 3-5 years sales experience in medical device or relevant industry * 1-2 years of people management experience, with proven success leading a sales team * Must ...
Regional Sales Manager-East
Raleigh, NC · On-site
Bachelor's Degree in related field * 3-5 years sales experience in medical device or relevant industry * 1-2 years of people management experience, with proven success leading a sales team * Must ...
This is a training position for someone who desires a career in Medical Device Sales * There will be opportunities to move up in the future BACKGROUND MUST HAVE: * Bachelor's degree required * The ...
This is a training position for someone who desires a career in Medical Device Sales * There will be opportunities to move up in the future BACKGROUND MUST HAVE: * Bachelor's degree required * The ...
The Kestra team has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders inspired by the opportunity to unite ...
The Kestra team has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders inspired by the opportunity to unite ...
This position is intended for an experienced engineer or industrial designer with a strong blend of medical device development discipline and consumer product design mindset . You will lead concept ...
This position is intended for an experienced engineer or industrial designer with a strong blend of medical device development discipline and consumer product design mindset . You will lead concept ...
FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745. This position provides technical documentation as required by U.S. Food and Drug ...
FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745. This position provides technical documentation as required by U.S. Food and Drug ...
Must have worked in a medical device company and familiar with regulatory and quality requirements throughout all stages of the product development life cycle. What You Will Do * Process Development ...
Must have worked in a medical device company and familiar with regulatory and quality requirements throughout all stages of the product development life cycle. What You Will Do * Process Development ...
FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745. This position provides technical documentation as required by U.S. Food and Drug ...
FDA) and European regulatory agencies under the EU Medical Device Regulation (EU MDR) - Regulation (EU) 2017/745. This position provides technical documentation as required by U.S. Food and Drug ...
Medical Device information
See Raleigh, NC salary details
$20.80 - $27.45
5% of jobs
$33.85 is the 25th percentile. Wages below this are outliers.
$27.45 - $34.10
21% of jobs
$34.10 - $40.74
21% of jobs
The median wage is $43.33 / hr.
$40.74 - $47.39
9% of jobs
$47.39 - $54.04
16% of jobs
$55.70 is the 75th percentile. Wages above this are outliers.
$54.04 - $60.69
11% of jobs
$60.69 - $67.34
6% of jobs
$67.34 - $73.99
7% of jobs
$73.99 - $80.64
2% of jobs
$80.64 - $87.29
1% of jobs
$87.29 - $93.94
0% of jobs
$20
$48
$93
How much do medical device jobs pay per hour?
What is a career in medical devices?
What medical device jobs pay the most?
What are the key skills and qualifications needed to thrive as a Medical Device Sales Representative, and why are they important?
What profession makes $400,000 a year?
What Are Different Types of Medical Device Jobs?
The healthcare industry relies on medical devices to treat and diagnose patients, so many jobs exist around medical devices as a result. A medical device engineer helps design medical devices to particular specifications during the research and design phase. A production specialist manufactures medical devices, while a QA inspector ensures that production adheres to Good Manufacturing Practice (GMP) regulations. A quality control technician ensures medical device function as intended. Finally, medical sales agents are responsible for medical device sales to healthcare providers and medical facilities.
What is the difference between Medical Device vs Medical Equipment Technician?
| Aspect | Medical Device | Medical Equipment Technician |
|---|---|---|
| Credentials | Certifications like Certified Biomedical Equipment Technician (CBET) | CBET or similar biomedical equipment certifications |
| Work Environment | Manufacturers, hospitals, clinics, research labs | Hospitals, clinics, service companies |
| Industry Usage | Design, development, regulation of medical devices | Maintenance, repair, calibration of medical equipment |
Medical Device professionals focus on the design, regulation, and development of medical devices, while Medical Equipment Technicians primarily handle maintenance, repair, and calibration of medical equipment. Both roles require similar certifications and often work in healthcare settings, but their core responsibilities differ significantly.
What are medical devices?
What are some typical challenges faced in a Medical Device sales role, and how can I prepare for them?
What jobs pay 10,000 a month without a degree?
- Manager Full Time Logistics
- 3Pl Warehouse Manager
- Seasonal Supply Chain Startup
- Medical Device Oem Manufacturer Sales
- Freelance Third Party Logistics
- Supply Chain Inventory Specialist
- Remote Supply Chain Logistics Faculty
- Warehouse And Logistics Manager
- Non Union Dsc Logistics
- Transportation Logistics Coordinator

Full-time
Posted 5 days ago
Job description
Are you ready to work for a more active world?
At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.
Bioventus LLC., seeks Senior Regulatory Affairs Specialist (Durham, NC).Duties:
- Author and submit applications 510(k), PMA Supplements and, Technical Documentation to receive product clearance / approvals for new products and maintain existing registrations globally.
- Author and maintain Technical Files compliant to the MDD 93/42/EEC and Technical Documentation compliant to the EU MDR 2017/745.
- Communicate with Regulatory Agencies regarding submissions, and changes of products, including manufacturing, design and new product development.
- Serve as Subject Matter Expert to represent Regulatory during internal audits and external audits by regulatory agencies.
- Review protocols and reports for scientific validity and compliance to regulatory standards and provide scientific judgement to guide cross functional teams.
- Perform Regulatory Assessments for design, manufacturing, and labeling changes to ensure compliance with regulations and standards where the product is registered.
- Research requirements and set priorities while maintaining project schedules. Provide guidance and oversight to team members related to regulatory compliance.
- Review marketing literature for compliance with applicable regulations and company policies and procedures.
Required: Master's degree or foreign equivalent in Regulatory Affairs, Pharmaceutical Sciences or related field plus 3 years of experience in the job offered, as Regulatory Engineer or related regulatory affairs position within the medical and/or diagnostic device industry.
Must have 3 years of experience with:
- Regulatory assessment of engineering/design change execution.
- Working with or providing guidance to cross-functional or offshore team in preparation of documents for regulatory agency submissions.
- Regulatory registrations in at least 3 or more of the following agencies or regions (FDA, EMEA, Canada, LATAM, Japan, Australia).
- Project management.
- Preparing and reviewing documentation regarding submissions and product changes of medical devices.
Must have experience working with medical device registrations compliant with Medical Device Regulation and EU Medical Device Directive.
Hybrid role model position, working 3 days in office and 2 days from within normal commuting distance of the office location.
National travel required 25% of the time.
Are you the top talent we are looking for?
Apply now! Hit the "Apply" button to send us your resume and cover letter.
Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms ofdiversity andtake pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation.All individuals, regardless of personal characteristics, are encouraged to apply.
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