1

Combination Product Medical Device Engineer Jobs in Raleigh, NC

... medical breakthrough for the treatment of neonatal respiratory distress syndrome (RDS) in the ... What is the role? The Procurement Manager - Drug and Device/Drug Combination Products is a ...

... combination product regulations, with awareness of ISO 13485. This person will establish ... Provide sponsor batch review and release of drug/biological product and oversight of medical device ...

Electrical Engineer - Contract Location: Durham, NC - Onsite Duration: 12-Month Contract Hours: 40 ... medical device products. You will contribute to various stages of the product lifecycle, from ...

Systems Verification & Validation Engineer, R&D (Medical Devices) This role focuses on leading ... product lifecycle. * Ensure compliance with relevant medical device industry regulations and ...

New

Systems Verification & Validation Engineer, R&D (Medical Devices) This role focuses on leading ... product lifecycle. * Ensure compliance with relevant medical device industry regulations and ...

New

Experience in a sterile or pharmaceutical environment is required but will consider other FDA -- cGMP experience and medical device or combination product production Performed validation of Quality ...

Be Seen First

C# Developer / Engineer

Raleigh, NC · On-site

$100K - $130K/yr

IEC 62304 - - Medical Device Software Standard - willing to learn * ISO 13485 - preferred * ISO ... Develop system software based on requirements for existing and new generation products * Develop ...

... medical devices/combination product development * Basic experience with coordination of GMP ... Preferred: * 5+ years in medical device manufacturing * Experience with quality operations, design ...

Senior Electrical Engineer

Raleigh, NC · On-site

$95K - $123K/yr

Delivering electrical and embedded products in a timely fashion with integrity and meeting all applicable standard for medical device quality. * Provide electrical and firmware engineering support ...

Senior Electrical Engineer

Raleigh, NC · On-site

$95K - $123K/yr

Delivering electrical and embedded products in a timely fashion with integrity and meeting all applicable standard for medical device quality. * Provide electrical and firmware engineering support ...

Senior Electrical Engineer

Raleigh, NC

$104K - $136K/yr

... new products meet Medical Device safety requirements such as IEC 60601 and other Medical Device standards. 4 Electrical Engineering • Ensure duties are completed according to client SOPs and ...

Manufacturing Engineer

Pittsboro, NC · On-site

$75 - $110/hr

... produce cost-effective quality medical device products and systems. * Provide support for ... Provide engineering expertise in resolving specific technology issues * Participate in ...

Showing results 21-40

Combination Product Medical Device Engineer information

See Raleigh, NC salary details

$51.5K

$140.1K

$199.3K

How much do combination product medical device engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for combination product medical device engineer in Raleigh, NC is $140,050.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,500.00 and $199,300.00 per year, depending on experience, location, and employer.

What is a combination product medical device engineer?

Combination Product Medical Device Engineers are professionals who design, develop, and oversee the manufacturing of medical products that integrate drugs, devices, and/or biological components. They ensure these products meet regulatory standards and function safely and effectively for patients. Their work often involves cross-disciplinary collaboration, detailed documentation, and rigorous testing to comply with FDA or other international requirements. These engineers play a crucial role in bringing innovative combination therapies and delivery systems to market.

What are some typical challenges faced by a combination product medical device engineer when working on cross-functional teams?

Combination Product Medical Device Engineers often collaborate with professionals from pharmaceutical, biotechnology, and device engineering backgrounds. One common challenge is ensuring clear communication across disciplines, as each team may have different regulatory requirements and technical needs. Balancing the integration of drug and device components while meeting strict FDA and ISO standards can also be complex. Proactively addressing these challenges through regular cross-functional meetings and thorough documentation helps ensure project success and compliance.

What are the key skills and qualifications needed to thrive as a combination product medical device engineer, and why are they important?

To thrive as a Combination Product Medical Device Engineer, you need a strong background in biomedical or mechanical engineering, familiarity with drug delivery systems, and experience in regulatory standards like FDA 21 CFR and ISO 13485. Proficiency with CAD software, risk management tools, and knowledge of quality management systems (QMS) are typically required, along with certifications such as Six Sigma or PMP being advantageous. Strong problem-solving abilities, attention to detail, and effective cross-functional communication are critical soft skills for excelling in this role. These competencies ensure the development of safe, compliant, and innovative combination products that meet both technical and regulatory requirements.

What is the difference between Combination Product Medical Device Engineer vs Medical Device Quality Engineer?

AspectCombination Product Medical Device EngineerMedical Device Quality Engineer
CredentialsBachelor's or higher in engineering, regulatory knowledgeBachelor's or higher, quality standards expertise
Work EnvironmentDesign, development, and testing of combination productsQuality assurance, compliance, and validation processes
Industry UsagePharmaceutical and medical device sectors involving combination productsMedical device manufacturing and regulatory compliance

The Combination Product Medical Device Engineer focuses on designing and developing products that integrate drugs, devices, or biologics, requiring cross-disciplinary skills. In contrast, the Medical Device Quality Engineer emphasizes ensuring product quality, compliance, and validation throughout manufacturing. Both roles are essential in the medical device industry but serve different stages of product lifecycle and expertise areas.

What are popular job titles related to Combination Product Medical Device Engineer jobs in Raleigh, NC?

For Combination Product Medical Device Engineer jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Combination Product Medical Device Engineer jobs in Raleigh, NC look for?

The top searched job categories for Combination Product Medical Device Engineer jobs in Raleigh, NC are:

Infographic showing various Combination Product Medical Device Engineer job openings in Raleigh, NC as of August 2026, with employment types broken down into 73% Full Time, 11% Part Time, and 16% Contract. Highlights an 79% In-person, 5% Hybrid, and 16% Remote job distribution, with an average salary of $140,050 per year, or $67.3 per hour.

Principal Engineer, Product Cybersecurity

Baxter

Raleigh, NC • On-site

$120K - $165K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 14 days ago


Key responsibilities

  • Own and direct the cybersecurity design and analysis of multiple medical devices.

  • Create, maintain, and analyze system requirements, architectures, risk analysis, and threat models related to medical device cybersecurity.

  • Perform vulnerability scanning, monitor threat intelligence, and drive cybersecurity improvements across cross-functional teams.


Job description

This is whereyour work makes a difference.

At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job-you will find purpose and pride.

Your Role at Baxter

This is where your work saves lives.

As Principal Engineer, own and direct the cybersecurity design and analysis of multiple medical devices. Demonstrate subject matter expert knowledge in state-of-the-art security principles. Resolve difficult problems, from conception to final design with team input. Plan, lead, and deliver project assignments in the evaluation, selection and adaptation of various cybersecurity engineering techniques, procedures, and criteria with minimal guidance.

Contributes to a cybersecurity vision that aligns with the organization's vision and strategic plan. Utilizes solid understanding of device and system connectivity concepts in a medical device domain. Provides direction to technical team members that are accountable for implementing cybersecurity, integration, and connectivity deliverables. Exhibits creativity and innovation in completing divisional and cross-functional/business unit goals and objectives.

What you'll be doing:

  • Implement proof of concept project to define innovative solutions on platforms/server platforms. Lead implementation of medical device cybersecurity principles as part of an overall security architecture.

  • Create, own, and maintain system requirements, architectures, risk analysis and other specifications that define the cybersecurity functionality of medical device systems both embedded and hosted.

  • Create threat models of medical device systems and the interfaces between medical devices.

  • Perform vulnerability scanning of medical device systems and analyze results.

  • Monitor threat intelligence and analyze CWEs and CVEs that affect medical device systems and propose solutions.

  • Drive cybersecurity improvements through product the cross functional teams, primarily software.

  • Lead discussions to resolve competing constraints between interrelated functions (Engineering, Risk Management, Compliance, Clinical, Human Factors, Regulatory, Marketing, Service).

  • Ensure compliance to the product development process and Quality System and Design Control requirements. Interface with regulatory bodies, representing Baxter and Baxter products, and ensure that regional cybersecurity needs are met.

What you'll bring

  • BS in computer science, engineering, mathematics, information management, or related field with 5+ years of industry experience or Masters with 3+ years.

  • Experience with threat modeling, penetration testing, fuzz testing, vulnerability scanning, secure code analysis.

  • Experience with cybersecurity related software such as Blackduck, Coverity, etc.

  • Experience dealing with threat intelligence, CWEs and CVEs.

  • Familiarity with cybersecurity related organizations and certifications such as UL (UL-2900), ICS-CERT, FIPS 140, etc.

  • Experience with cybersecurity functionality on embedded systems and hosted software applications.

  • Requires strong organization and communication skills, with the ability to interface with both technical and non-technical personnel.

  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods.

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $120,000 to $165,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

#LI-MS1

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees.For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Know Your Rights: Workplace Discrimination is Illegal

Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.