1

Freelance Quality Engineer Fda Jobs in Delaware (NOW HIRING)

Product Quality Engineer 2

Newark, DE · On-site

$78K - $122K/yr

Strong understanding of FDA Quality System Regulations, including Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with ...

Product Quality Engineer 2

Newark, DE · On-site

$78K - $122K/yr

Strong understanding of FDA Quality System Regulations, including Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with ...

Strong understanding of FDA Quality System Regulations, including Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with ...

Product Quality Engineer 2

Newark, DE · On-site

$78K - $122K/yr

Strong understanding of FDA Quality System Regulations, including Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP. * Familiarity with ...

Provide product quality engineering support for on-market medical devices. This role will be ... Experience in an FDA regulated industry preferred Experience in root cause analysis or product ...

Product Quality Engineer 2

Newark, DE · On-site

$78 - $122/hr

Provide product quality engineering support for on-market medical devices. This role will be ... Experience in an FDA regulated industry preferred * Experience in root cause analysis or product ...

Product Quality Engineer 2

Newark, DE · On-site

$78K - $122K/yr

Provide product quality engineering support for on-market medical devices. This role will be ... Experience in an FDA regulated industry preferred Experience in root cause analysis or product ...

Product Quality Engineer 1

Newark, DE · On-site

$54K - $86K/yr

Provide product quality engineering support for on-market medical devices. This role will be ... Experience in an FDA regulated industry preferred Experience in root cause analysis or product ...

Provide product quality engineering support for on-market medical devices. This role will be ... Experience in an FDA regulated industry preferred Experience in root cause analysis or product ...

Product Quality Engineer 3

Newark, DE · On-site

$85K - $133K/yr

Product Quality Engineer will make a direct impact on patient safety and product excellence by ... Skills * Working knowledge of FDA Quality System Regulations, especially Design Control ...

Product Quality Engineer 3

Newark, DE · On-site

$85K - $133K/yr

Product Quality Engineer will make a direct impact on patient safety and product excellence by ... Skills * Working knowledge of FDA Quality System Regulations, especially Design Control ...

Product Quality Engineer 3

Newark, DE · On-site

$85.30 - $133/hr

Job Summary Product Quality Engineer will make a direct impact on patient safety and product ... Skills * Working knowledge of FDA Quality System Regulations, especially Design Control ...

Quality Design Engineer 2

Newark, DE · On-site

$78K - $122K/yr

The Quality Design Engineer II is responsible for executing design changes, product enhancements ... Support completion of Design History File documentation per FDA and other compliance requirements.

Quality Design Engineer 2

Newark, DE · On-site

$78K - $122K/yr

Skills • Experience with FDA Quality Systems Regulation, especially Design Control requirements ... per engineering discipline. • Strong knowledge of Good Laboratory Practices and QSR (Quality ...

CAPA Facilitator, Engineer

Newark, DE · On-site

$98 - $153/hr

Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and ... FDA inspections, as a CAPA and quality systems subject matter expert. * Assist with audit ...

CAPA Facilitator, Engineer

Newark, DE · On-site

$97K - $152K/yr

Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and ... FDA inspections, as a CAPA and quality systems subject matter expert. * Assist with audit ...

CAPA Facilitator, Engineer

Newark, DE · On-site

$97K - $152K/yr

Hologic is seeking a Quality Engineer, CAPA Facilitator to support and strengthen Corrective and ... FDA inspections, as a CAPA and quality systems subject matter expert. * Assist with audit ...

Katalyst CRO is looking for a QA Engineer with Life Sciences domain experience to support testing ... FDA, and 21 CFR Part 11 regulations. • Collaborate with cross-functional teams in an Agile ...

next page

Showing results 1-20

Freelance Quality Engineer Fda information

What does a freelance quality engineer FDA do?

A Freelance Quality Engineer FDA is a professional who works independently to help companies comply with FDA regulations, particularly in industries like medical devices, pharmaceuticals, and biotechnology. They are responsible for ensuring that products and processes meet all quality and safety standards set by the FDA. Their tasks may include auditing, creating and reviewing documentation, implementing quality management systems, and assisting with regulatory submissions. By working on a contract basis, they provide specialized expertise to organizations that may not require a full-time quality engineer.

What are the key skills and qualifications needed to thrive as a freelance quality engineer FDA?

To thrive as a Freelance Quality Engineer FDA, you need a solid background in quality assurance, regulatory compliance, and FDA guidelines, often supported by a degree in engineering or life sciences. Familiarity with tools such as quality management systems (QMS), CAPA software, and experience with ISO 13485 or similar certifications is crucial. Strong analytical thinking, attention to detail, and effective communication skills set top professionals apart in this field. These competencies are essential for ensuring product safety, regulatory adherence, and maintaining client trust in the highly regulated medical device and pharmaceutical industries.

What are some common challenges faced by freelance quality engineers working with FDA-regulated products?

Freelance Quality Engineers working in FDA-regulated environments often encounter challenges such as staying up-to-date with evolving FDA regulations, ensuring thorough documentation for audits, and quickly adapting to each client's unique quality management systems. They may also face tight project timelines and the need to communicate effectively with cross-functional teams, including regulatory, manufacturing, and R&D personnel. Building strong relationships and maintaining clear, consistent documentation are essential strategies for overcoming these challenges and delivering successful project outcomes.

What is the difference between Freelance Quality Engineer Fda vs Freelance Quality Assurance Specialist?

AspectFreelance Quality Engineer FdaFreelance Quality Assurance Specialist
CertificationsFDA regulations, ISO standards, QA certificationsISO standards, QA certifications, industry-specific credentials
Work EnvironmentMedical device, pharmaceutical, biotech industriesManufacturing, software, consumer products industries
Employer & Industry UsageRegulated industries requiring FDA complianceVarious industries focusing on quality processes
Common Search & Comparison IntentUnderstanding FDA-specific quality rolesComparing QA roles across industries

Freelance Quality Engineer Fda primarily focuses on ensuring compliance with FDA regulations in regulated industries like pharmaceuticals and medical devices. Freelance Quality Assurance Specialist covers broader quality assurance tasks across various sectors. While both roles require QA certifications, the FDA-specific role emphasizes regulatory knowledge, making it ideal for those targeting FDA-regulated industries.

What are popular job titles related to Freelance Quality Engineer Fda jobs in Delaware?

For Freelance Quality Engineer Fda jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Freelance Quality Engineer Fda jobs in Delaware look for?

The top searched job categories for Freelance Quality Engineer Fda jobs in Delaware are:

What cities in Delaware are hiring for Freelance Quality Engineer Fda jobs?

Cities in Delaware with the most Freelance Quality Engineer Fda job openings:

Infographic showing various Freelance Quality Engineer Fda job openings in Delaware as of July 2026, with employment types broken down into 1% Locum Tenens, 91% Full Time, 5% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution.

Product Quality Engineer 2

Newark, DE • On-site


Hologic Inc.
5 - 10K employees

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

181st of 495 rated machine equipment manufacturers

Good employer

Recommended by parents

Respectful managers


$78K - $122K/yr

Full-time

Re-posted 12 days ago


Job description

Are you passionate about ensuring the quality and reliability of life-saving medical devices? At Hologic, we are seeking a Product Quality Engineer 2  to provide engineering support for on-market medical devices. In this role, you'll lead complaint investigations, perform root cause analyses, and implement corrective and preventive actions to improve product quality and compliance. Collaborating with cross-functional teams, you'll drive process improvements, assess risks, and deliver impactful solutions that enhance patient safety and customer satisfaction. If you're a proactive problem-solver with a strong background in quality engineering, we encourage you to apply and make a difference in healthcare innovation.

Knowledge:

  • Strong understanding of FDA Quality System Regulations, including Design Control requirements, ISO 13485, EU Medical Device Regulation, ISO 14971 (Risk Management), GMP, and GDP.
  • Familiarity with root cause analysis tools, risk management principles, and compliance frameworks.
  • Preferred knowledge of test method validation, statistical methods, design of experiments (DOE), and industry standards related to reliability, sterilization, packaging, and biocompatibility.

Skills:

  • Proven ability to lead complaint investigations, root cause analyses, and CAPA activities to resolve quality issues.
  • Strong data analysis and trending skills to identify risks, assess failure modes, and recommend mitigations.
  • Effective communication and presentation skills to articulate findings, root causes, and recommendations to stakeholders and leadership.
  • Ability to assess product changes for design and risk management impact, ensuring compliance and quality standards are maintained.
  • Proficiency in developing or improving testing methods for complaint investigations and technical activities.
  • Experience collaborating with cross-functional teams, including Operations, R&D, and Engineering, to drive product and process improvements.
  • Preferred: Familiarity with verification and validation requirements and the development of testable and measurable specifications.

Behaviors:

  • Detail-oriented and compliance-focused, ensuring adherence to regulatory standards and quality system requirements.
  • Proactive and results-driven, with a strong sense of ownership for deliverables and outcomes.
  • Collaborative and team-oriented, building productive relationships across functions to drive quality improvements.
  • Customer-focused, with a commitment to addressing field quality issues and ensuring timely resolution.
  • Continuous improvement mindset, driving process optimization and identifying opportunities to enhance product quality.

Experience:

  • Bachelor's degree in Engineering (Mechanical, Biomedical, Biomechanical, Electrical, or related discipline) required.
  • 2-5 years of experience in quality engineering, product development, or R&D, preferably in an FDA-regulated industry.
  • Hands-on experience in complaint investigations, root cause analysis, and CAPA activities.
  • Familiarity with internal and external audits, including Notified Body and FDA inspections.


Why join Hologic?
We are committed to making Hologic the destination for top talent. 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.
The annualized base salary range for this role is $78,000-$122,100 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, 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.

#LI-NT1



What Hologic employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom