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Contract Quality Engineer Medical Device Jobs in Boca Raton, FL

atrion

Quality Engineer

Davie, FL

$66K - $85K/yr

Provide quality engineering support to engineering project teams associated with new product ... A minimum of 5 years' experience in the medical device manufacturing industry is preferred.

iMPact Business Group

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Medical Device Inspector-27596

Weston, FL · On-site

$23/hr

This is a 12+ month contract opportunity within a highly collaborative, quality-focused manufacturing environment. The Medical Device Inspector II will perform dimensional, visual, and electrical ...

atrion

Quality Engineering Manager

Davie, FL

Excellent working knowledge of medical device regulations and industry standards pertaining to ... ASQ Certified Quality Manager or Certified Quality Engineer * ISO 13485 Lead Auditor * Lean Six ...

Workila

Sr. Quality Engineer

Fort Lauderdale, FL · On-site

$84K - $114K/yr

Bachelor's degree or higher (engineering/science) * 3+ yrs quality engineering w/ 1+ yrs Med device industry * Know GD&T, Solidworks (read drawings), root cause analysis and CAPA * Can move NC from ...

Medical Device Distribution Company

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Product Quality Inspection Specialist

Miami Gardens, FL · On-site

$70K - $80K/yr

... Engineering Technology, Physical Sciences, or another technical discipline directly related to manufactured products. * Minimum 3-5 years of professional quality experience within medical device ...

Quality

Complaints Engineer II - TA

Sunrise, FL · Hybrid

Provide engineering expertise for complaint-investigation test equipment, including feasibility ... At least three years of experience in medical-device quality assurance or a clinical environment.

New

Medical Device Distribution Company

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Product Quality Inspection Specialist

Miami Gardens, FL · On-site

$70K - $80K/yr

... Engineering Technology, Physical Sciences, or another technical discipline directly related to manufactured products. * Minimum 3-5 years of professional quality experience within medical device ...

SV Microwave

Quality Engineer

West Palm Beach, FL · On-site

$69K - $90K/yr

Minimum 2 years of experience as a Quality Engineer in a manufacturing environment (aerospace ... Complete benefit package includes medical, dental, vision, disability, life insurance, student loan ...

SV Microwave

Quality Engineer

West Palm Beach, FL · On-site

$70 - $110/hr

Minimum 2 yearsof experience as a Quality Engineer in a manufacturing environment (aerospace ... Complete benefit package includes medical, dental, vision, disability, life insurance, student ...

SV Microwave

Quality Engineer

West Palm Beach, FL · On-site

$69K - $90K/yr

Minimum 2 years of experience as a Quality Engineer in a manufacturing environment (aerospace ... Complete benefit package includes medical, dental, vision, disability, life insurance, student loan ...

Sv-Microwave-1

Quality Engineer

West Palm Beach, FL · On-site

$70 - $110/hr

Minimum 2 yearsof experience as a Quality Engineer in a manufacturing environment (aerospace ... Complete benefit package includes medical, dental, vision, disability, life insurance, student ...

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Showing results 1-20

All JobsContract Quality Engineer Medical Device JobsContract Quality Engineer Medical Device Jobs in Boca Raton, FL

Contract Quality Engineer Medical Device information

See Boca Raton, FL salary details

$42.7K

$79.8K

$112.9K

How much do contract quality engineer medical device jobs pay per year?

As of Aug 26, 2026, the average yearly pay for contract quality engineer medical device in Boca Raton, FL is $79,750.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,300.00 and $88,300.00 per year, depending on experience, location, and employer.

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

A Contract Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory and company quality standards during a specific project or timeframe. They typically work on a contract basis, focusing on tasks like process validation, risk management, root cause analysis, and compliance with standards such as ISO 13485 and FDA regulations. Their role often involves collaborating with engineering, production, and regulatory teams to troubleshoot quality issues and implement corrective actions. They play a key role in maintaining product safety and regulatory compliance throughout the manufacturing process.

What are the key skills and qualifications needed to thrive as a contract quality engineer in the medical device industry?

To thrive as a Contract Quality Engineer in the Medical Device field, you need expertise in quality assurance, regulatory compliance (such as ISO 13485 and FDA regulations), and a background in engineering or life sciences. Familiarity with tools like CAPA systems, risk management software, and proficiency in quality management systems (QMS) is typically required. Strong analytical thinking, attention to detail, and effective communication skills set top performers apart in this role. These skills are essential to ensure product safety, regulatory compliance, and the successful launch and maintenance of medical devices in a highly regulated environment.

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

As a Contract Quality Engineer in the medical device sector, you will frequently work closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and supply chain. Your responsibilities often involve reviewing design documentation, participating in risk assessments, and ensuring production processes meet both internal quality standards and regulatory requirements. Effective communication is key, as you'll be responsible for conveying quality expectations, addressing non-conformities, and supporting project timelines. This collaborative environment provides valuable experience in coordinating with diverse professionals while upholding strict industry standards.

What is the difference between Contract Quality Engineer Medical Device vs Contract Quality Engineer Pharmaceutical?

AspectContract Quality Engineer Medical DeviceContract Quality Engineer Pharmaceutical
CertificationsISO 13485, FDA QSR, GMPICH Q7, GMP, FDA regulations
Work EnvironmentMedical device manufacturing, labs, compliance auditsPharmaceutical production, labs, quality assurance
Industry UsageMedical device companies, OEMs, suppliersPharmaceutical firms, biotech companies, contract manufacturers

Both roles focus on quality assurance and regulatory compliance but differ mainly in industry-specific standards and environments. Contract Quality Engineers Medical Device work primarily with ISO 13485 and FDA QSR standards in device manufacturing, while Contract Quality Engineers Pharmaceutical focus on GMP and ICH Q7 regulations in drug production. Understanding these differences helps candidates target the right industry and certifications for their career goals.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Boca Raton, FL?

The most popular types of Quality Engineer Medical Device jobs in Boca Raton, FL are:

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For Contract Quality Engineer Medical Device jobs in Boca Raton, FL, the most frequently searched job titles are:

What job categories do people searching Contract Quality Engineer Medical Device jobs in Boca Raton, FL look for?

The top searched job categories for Contract Quality Engineer Medical Device jobs in Boca Raton, FL are:

What cities near Boca Raton, FL are hiring for Contract Quality Engineer Medical Device jobs?

Cities near Boca Raton, FL with the most Contract Quality Engineer Medical Device job openings:

Contract Quality Engineer Medical Device jobs near you

Quality Control Technician (Quality Engineer)

Ubertal Inc

Boca Raton, FL • Remote

Contractor

Re-posted 7 days ago

Job description

Job Title: Quality Control Technician (Quality Engineer – Contract)

Location: 100% Remote (Preferred Eastern or Central Time Zones)
Duration: 12 Months
Schedule: Full-Time, 40 Hours/Week | Standard Business Hours
Conversion: No FTE conversion available
Interview Process: 1 Round

We are seeking an experienced Quality Control Technician with strong validation and quality systems expertise to support documentation, statistical quality control, and regulatory compliance initiatives in a highly regulated pharmaceutical or manufacturing environment.

This role focuses on validation documentation, quality analysis, regulatory compliance, and cross-functional collaboration to ensure systems, products, and processes meet defined reliability and regulatory standards.

Key Responsibilities:

  • Write, review, approve, and execute validation documentation and technical reports for systems, products, and processes

  • Prepare validation protocols, test equipment, and evaluate validation data

  • Conduct statistical quality control analysis of testing results and process anomalies

  • Prepare reports summarizing study results and conformance to acceptance criteria

  • Support development and maintenance of validation programs and Standard Operating Procedures (SOPs)

  • Verify calibration, maintenance, and repair of instruments supporting Quality Systems validation

  • Participate in FMEA, RCA, and CAPA development activities

  • Ensure corrective and preventive measures meet reliability and compliance standards

  • Maintain working knowledge of FDA, CLIA, cGMP, Medical Device Directives, and other applicable regulatory standards

  • Support procedural document management and regulatory audit readiness

  • Communicate cross-functionally regarding validation studies and project deliverables

Required Qualifications:

  • Bachelor’s degree in Science, Engineering, or related field (or equivalent combination of education and relevant experience)

  • Minimum 3 years of quality/validation experience in pharmaceutical manufacturing or a highly regulated industry

  • Strong working knowledge of cGMP principles and regulatory compliance requirements

  • Experience writing and approving validation and technical documentation

  • Experience participating in FMEA, RCA, and CAPA processes

  • Strong analytical, critical thinking, and problem-solving skills

  • Project management skills with ability to manage multiple priorities and tight deadlines

  • Proficiency in Microsoft Office, statistical tools, and electronic quality systems

  • Strong written, verbal, and interpersonal communication skills

  • Ability to maintain confidentiality and demonstrate professional judgment

Preferred Qualifications:

  • ASQ Certification

  • Experience in medical device or regulated laboratory environments

This remote contract opportunity is ideal for a quality professional with deep validation experience, strong regulatory knowledge, and the ability to drive compliance and quality excellence within a regulated pharmaceutical or manufacturing environment.