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Medical Device Jobs in Raleigh, NC (NOW HIRING)

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.

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 ...

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 ...

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 ...

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 ...

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 ...

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Medical Device information

See Raleigh, NC salary details

$20

$48

$93

How much do medical device jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for medical device in Raleigh, NC is $48.45, according to ZipRecruiter salary data. Most workers in this role earn between $34.13 and $57.93 per hour, depending on experience, location, and employer.

What is a career in medical devices?

A career in medical devices involves designing, manufacturing, testing, and maintaining medical equipment such as diagnostic tools, surgical instruments, and implantable devices. Professionals in this field often require knowledge of engineering, biology, or healthcare regulations, and may need certifications or training to ensure safety and compliance in a clinical environment.

What medical device jobs pay the most?

Senior roles in medical device manufacturing, such as Regulatory Affairs Directors, Quality Assurance Managers, and R&D Directors, tend to have the highest salaries. These positions often require advanced degrees, extensive experience, and specialized certifications, and they typically involve leadership responsibilities in product development, compliance, or quality management.

What are the key skills and qualifications needed to thrive as a Medical Device Sales Representative, and why are they important?

To thrive as a Medical Device Sales Representative, you need a strong background in sales, knowledge of medical terminology, and typically a bachelor's degree in life sciences or a related field. Familiarity with CRM software, product demonstration tools, and relevant certifications such as Certified Sales Professional (CSP) are commonly required. Exceptional communication, relationship-building, and negotiation skills help you connect with healthcare professionals and address their needs effectively. These skills are vital for successfully promoting products, meeting sales targets, and ensuring customer satisfaction in a highly regulated industry.

What profession makes $400,000 a year?

In the medical device industry, senior roles such as Vice President of Medical Devices or Chief Medical Officer can earn $400,000 or more annually, especially with extensive experience, advanced degrees, and leadership responsibilities. High-level executives and specialized engineers in this field often reach this compensation level through bonuses and stock options.

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?

AspectMedical DeviceMedical Equipment Technician
CredentialsCertifications like Certified Biomedical Equipment Technician (CBET)CBET or similar biomedical equipment certifications
Work EnvironmentManufacturers, hospitals, clinics, research labsHospitals, clinics, service companies
Industry UsageDesign, development, regulation of medical devicesMaintenance, 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?

Medical devices are instruments, machines, implants, or related articles used to diagnose, prevent, monitor, or treat medical conditions and diseases in humans. They range from simple items like bandages and thermometers to complex technologies such as pacemakers, MRI machines, and surgical robots. Medical devices play a crucial role in healthcare by improving patient outcomes, supporting medical professionals, and enhancing the quality of life. They are regulated to ensure safety and effectiveness before being approved for use.

What are some typical challenges faced in a Medical Device sales role, and how can I prepare for them?

Medical Device sales professionals often encounter challenges such as navigating complex regulatory requirements, staying updated on evolving product technologies, and building relationships with healthcare providers who have demanding schedules. Success in this field relies on strong communication skills, persistence, and a continuous learning mindset. To prepare, familiarize yourself with the latest industry regulations, actively seek product training, and develop strategies for effective time management and customer engagement.

What jobs pay 10,000 a month without a degree?

In the medical device industry, roles such as sales representatives, technical specialists, or product trainers can sometimes earn around $10,000 per month through commissions, bonuses, or experience. These positions often require strong communication skills, industry knowledge, and certifications rather than formal degrees, and may involve travel or working in clinical environments.
What are the most commonly searched types of Medical Device jobs in Raleigh, NC? The most popular types of Medical Device jobs in Raleigh, NC are:
What are popular job titles related to Medical Device jobs in Raleigh, NC? For Medical Device jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Medical Device jobs? Cities near Raleigh, NC with the most Medical Device job openings:
Infographic showing various Medical Device job openings in Raleigh, NC as of June 2026, with employment types broken down into 50% Part Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $100,768 per year, or $48.4 per hour.

Senior Regulatory Affairs Specialist

Osv_bioventus

Durham, NC • Hybrid

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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