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Freelance Quality Engineer Fda Jobs (NOW HIRING)

Zobility

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Freelance Quality Inspector (Junior engineer / retired engineer)

Rockford, IL · On-site

We need good Freelance Quality Inspector or even a good Quality engineer (either junior or retired) who is oriented towards carrying out inspections. There will be lot of engineering topics to also ...

Stark Pharma Solutions Inc

Quality Engineer

Cambridge, MA · On-site

$78K - $101K/yr

Quality Engineer Location: Cambridge , MA Industry: Medical Device / Pharmaceutical Job Summary We ... Support Quality Management System (QMS) activities and ensure compliance with FDA, cGMP, and ISO ...

Actalent

Quality Engineer

Fort Wayne, IN

$66K - $85K/yr

Maintain complete and accurate CAPA documentation in accordance with ISO standards, FDA Quality System Regulations (QSR), and internal quality system requirements. * Interpret engineering drawings ...

LaborMax - Olive Branch, MS

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Quality Engineer

Olive Branch, MS · On-site

$85K - $100K/yr

Quality Engineer - Medical Device Manufacturing Location: Olive Branch, MS Job Type: Full-Time Join ... Maintain documentation in compliance with ISO 13485, FDA 21 CFR Part 820, FDA 21 CFR Part 1271, and ...

Stark Pharma Solutions Inc

Quality Engineer

Newark, NJ · On-site

$75K - $97K/yr

Quality Engineer Location: New Jersey Duration: Long Term Position Overview We are seeking an ... This role will focus on ensuring compliance with FDA regulations, cGMP requirements, quality system ...

Actalent

Quality Engineer

Dallas, TX

$30 - $38/hr

The Quality Engineer I will be responsible for supporting and improving Quality Management System ... Maintain compliance with FDA Quality System Regulation, cGMP requirements, ISO 13485, ISO 9001, and ...

Flotec

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Quality Engineer

Avon, IN · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Manufacturing Company Overview Flotec is an Indianapolis-based ... Support and maintain compliance with ISO 13485, FDA QSR, and applicable medical device regulatory ...

Generis TEK Inc.

Quality Engineer

Pleasanton, CA · On-site

$34.50/hr

Position Details: Quality Engineer - Pleasanton, CA Location : Pleasanton, CA 94588 Project ... S. Food and Drug Administration (FDA) regulations, other regulatory requirements including ISO ...

Iridex Corporation

Quality Engineer

Mountain View, CA · On-site

$112K - $120K/yr

Strong working knowledge of FDA 21 CFR 820, ISO 13485, MDSAP, MDR and ISO 14971, and applicable ... ASQ Certified Quality Engineer (CQE) or equivalent certification is preferred. * Strong problem ...

Iridex Corporation

Quality Engineer

Mountain View, CA

$112K - $120K/yr

Strong working knowledge of FDA 21 CFR 820, ISO 13485, MDSAP, MDR and ISO 14971, and applicable ... ASQ Certified Quality Engineer (CQE) or equivalent certification is preferred. * Strong problem ...

Iridex Corporation

Quality Engineer

Mountain View, CA · On-site

$112K - $120K/yr

Strong working knowledge of FDA 21 CFR 820, ISO 13485, MDSAP, MDR and ISO 14971, and applicable ... ASQ Certified Quality Engineer (CQE) or equivalent certification is preferred. * Strong problem ...

Bradford Soap Works Inc

Quality Engineer

West Warwick, RI · On-site

$69K - $90K/yr

Job Title: Quality Engineer Reports to: Quality Operations Manager Job Function: The Quality ... Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and ...

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Freelance Quality Engineer Fda information

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How much do freelance quality engineer fda jobs pay per year?

As of Jul 27, 2026, the average yearly pay for freelance quality engineer fda in the United States is $84,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $93,000.00 per year, depending on experience, location, and employer.

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 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 are the key skills and qualifications needed to thrive as a Freelance Quality Engineer FDA, and why are they important?

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 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.
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What cities are hiring for Freelance Quality Engineer Fda jobs? Cities with the most Freelance Quality Engineer Fda job openings:
What are the most commonly searched types of Quality Engineer Fda jobs? The most popular types of Quality Engineer Fda jobs are:
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Freelance Quality Engineer Fda jobs near you
Infographic showing various Freelance Quality Engineer Fda job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 95% Full Time, 1% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.
Freelance Quality Inspector (Junior engineer / retired engineer)

Freelance Quality Inspector (Junior engineer / retired engineer)

Zobility

Rockford, IL • On-site

Contractor

Medical, Dental, PTO

Posted 3 days ago

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Job description


We need good Freelance Quality Inspector or even a good Quality engineer (either junior or retired) who is oriented towards carrying out inspections.

There will be lot of engineering topics to also inspect as a part of ONSOURCE INSPECTION.

on source inspector Stamping part supplier

Position: Source Inspector (Stamping Parts Supplier

Job Summary:
Perform source inspections at metal stamping suppliers to ensure parts comply with engineering drawings, quality standards, and purchase order requirements before shipment. Verify product conformity, documentation, and supplier process compliance to support on-time delivery of defect-free components.

Key Responsibilities:

  • Conduct source inspections at supplier facilities for stamped metal parts.
  • Review engineering drawings, GD&T, specifications, and quality requirements.
  • Perform dimensional, visual, and functional inspections using precision measuring tools (calipers, micrometers, height gauges, CMM, etc.).
  • Verify First Article Inspection (FAI), PPAP (if applicable), Certificates of Conformance (CoC), and inspection records.
  • Ensure compliance with AS9100/ISO 9001, customer requirements, and quality procedures.
  • Identify non-conformances, document inspection findings, and coordinate corrective actions with suppliers and SQEs.
  • Approve or reject parts for shipment based on inspection results.
  • Support supplier quality improvement, root cause analysis, and CAPA activities.
  • Prepare source inspection reports and communicate quality status to Procurement and Quality teams.

Company Description

Zobility is RGBSI's workforce management and staffing division. RGBSI is a multi-national corporation headquartered in Troy, MI with branches throughout the USA, Canada, Germany, and India.