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Quality Engineer Medical Devices Jobs in Delaware

Staff Engineer, Quality

Newark, DE

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE · On-site

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE · On-site

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE · On-site

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE · On-site

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE · On-site

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Staff Engineer, Quality

Newark, DE

$70K - $91K/yr

Partner with Manufacturing, Process Engineering, and R&D teams to improve product quality, process capability, and manufacturing performance * Spend significant time on the manufacturing floor ...

Experience * 2-5+ years of quality engineering experience in a regulated manufacturing environment , preferably medical device, pharmaceutical, or healthcare packaging . * Experience with molding or ...

Experience * 2-5+ years of quality engineering experience in a regulated manufacturing environment , preferably medical device, pharmaceutical, or healthcare packaging . * Experience with molding or ...

Quality Design Engineer 2

Newark, DE · On-site

$78K - $122K/yr

The Quality Design Engineer II is responsible for executing design changes, product enhancements ... 14971 (Risk Management), and Medical Devices Directive. Ability to work effectively and ...

Quality Design Engineer 2

Newark, DE · On-site

$78K - $122K/yr

The Quality Design Engineer II is responsible for executing design changes, product enhancements ... Risk Management), and Medical Devices Directive. • Ability to work effectively and ...

Showing results 21-40

Quality Engineer Medical Devices information

See Delaware salary details

$45K

$84.1K

$119.1K

How much do quality engineer medical devices jobs pay per year?

As of Aug 12, 2026, the average yearly pay for quality engineer medical devices in Delaware is $84,111.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $93,100.00 per year, depending on experience, location, and employer.

What does a quality engineer do in the medical device industry?

A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.

How does a quality engineer collaborate with cross-functional teams in the medical device industry?

Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.

What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?

AspectQuality Engineer Medical DevicesQuality Technician Medical Devices
CertificationsISO 13485, Six Sigma, ASQ certificationsISO 13485, basic quality certifications
ResponsibilitiesDesigning quality systems, process improvements, root cause analysisInspecting products, conducting tests, recording quality data
Work EnvironmentDesign and development labs, manufacturing plantsManufacturing floors, quality control labs
Employer & Industry UsageMedical device companies, OEMs, suppliersManufacturers, contract labs, quality departments

In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?

To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.
What are popular job titles related to Quality Engineer Medical Devices jobs in Delaware? For Quality Engineer Medical Devices jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Quality Engineer Medical Devices jobs in Delaware look for? The top searched job categories for Quality Engineer Medical Devices jobs in Delaware are:
What cities in Delaware are hiring for Quality Engineer Medical Devices jobs? Cities in Delaware with the most Quality Engineer Medical Devices job openings:
Infographic showing various Quality Engineer Medical Devices job openings in Delaware as of August 2026, with employment types broken down into 3% As Needed, 83% Full Time, 3% Part Time, and 11% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $84,111 per year, or $40.4 per hour.

Senior Software Engineer, Medical Device

Hologic Inc.

Newark, DE • On-site

$119K - $157K/yr

Full-time

Re-posted 2 days ago


Hologic rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

175th of 487 rated machine equipment manufacturers


Job description

Located in Newark, DE, Hologic's Innovation Center is continuing to offer job opportunities. We are seeking a Senior Software Engineer (C#/ .NET, Full Stack) to design, develop, troubleshoot, and debug software for new and existing products.

The person in this role will work as part of a team developing user-facing applications for medical devices related to breast and skeletal health. This team currently works to support applications using C#, WPF, .NET, Java and Android, for clinical and internal users.

In addition to technical skills, we are looking for someone to be a strong technical leader on this team. They should deeply understand and adhere to good coding practices and be able to effectively mentor junior engineers. We expect them to partner with management to improve team processes and efficiency. The most successful person in this role exhibits a high degree of technical excellence, is collaborative, and takes initiative to do what's best for the product and customer. 

While the ideal candidate would be able to work onsite full time, we are open to discuss hybrid flexibility for the right candidate. 

At Hologic we are committed to creating groundbreaking technology that enables healthier lives everywhere, every day. We strive to become global champions for women's health by delivering dependable technology that saves lives. Apply today and join a purpose you will be proud to stand behind.

Role Expectations

  • Develop an expert level of understanding of our products and their use in clinical practice, to maintain, design, develop and test them.
  • Design and develop high quality software. 
  • Develop and maintain software under an Agile/Scrum/Continuous Integration methodology.
  • Contribute to technical documentation of new product , features, and functionality.
  • Identify, design, and implement appropriate software testing.
  • Collaborate with Test Engineers to understand functionality for the development and support of testing plans.
  • Identify, diagnose, prioritize, and resolve technical issues. 
  • Analyze defects, provide feedback, and implement process improvements. 
  • Train external teams on key product design elements, their operation, and how to use them properly.
  • Apply and share knowledge of new and emerging technologies and continually seek opportunities for potential product improvements.
  • Act as a technical leader by continuously searching for potential product improvements and insisting on the highest levels of product quality and usability.
  • Define and develop product improvements and new features in collaboration with Product Management and Domain Experts. 
  • Perform software risk assessments (ex: FMEAs); evaluate and develop risk mitigations as applicable to component, subsystem, and system level testing.

Skills

  • Expert understanding of computer science concepts, including operating systems, databases, software systems, and networking.
  • Expert programming skills, including Object-Oriented coding skills in .NET/C#, C++, C, Java or similar language. 
  • Demonstrated mastery of software design principles, algorithms, data structures, and multithreading concepts. Ability to recognize and leverage design patterns.
  • Ability to architect software, defining the high-level structure of a complex software system, to meet functional & performance needs and support future maintainability.
  • Strong debugging skills; Experienced in troubleshooting and resolving complex issues.
  • Ability to work with & contribute to appropriate technical documentation (ex: software requirement specifications, software design documentation, release notes, etc.)
  • Ability to conduct and participate in effective, thorough code reviews.
  • Strong familiarity with developer tooling, including version control , CICD build pipelines, and issue & project tracking tools. 
  • Excellent written and verbal communication skills, particularly in communicating complex technical details with both technical and non-technical audiences. 
  • Ability to adapt communication style to suit different audiences. 
  • Strong contributor to high performing team. 
  • Demonstrate ownership in executing project plans and meeting deadlines. 
  • Strong awareness of both local and system-level impact of code written.
  • Ability to provide feedback on requirements and test cases for completeness, accuracy, and ability to implement and test. 
  • Ability to support & drive departmental best practices and product or process improvements. 
  • Familiarity & experience with secure coding principles or cybersecurity is a plus.
  • Medical device experience is a plus. 
  • Medical imaging/general image processing is a plus. 
  • Understanding DICOM/HL7 is a plus. 

 Education

  • Preferred Minimum Technical/Advanced Degree: Technical Bachelor's or Master's Degree in a related field. 

Technical Experience

  • Bachelors Degree - 5-8 yrs 
  • Masters Degree - 4-6 yrs

So why join Hologic?

We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and an annual bonus scheme, one of our talent partners can discuss this in more detail with you.

If you have the right skills and experience and want to join our team, apply today. We can't wait to hear from you!

The annualized base salary range for this role is $106,500 - $166,600 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.

Agency and Third-Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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