2

Remote Supplier Quality Engineer Jobs in Boca Raton, FL

Sr Data Engineer

Plantation, FL ยท Remote

$109K - $131K/yr

... quality data solutions. Additionally, this role is expected to clearly communicate technical ... TYPICAL WORKING CONDITIONS โ€ข Full time remote/telework OTHER PHYSICAL REQUIREMENTS โ€ข Vision โ€ข ...

Azure Cloud Data Engineer

Weston, FL ยท Remote

$108K - $130K/yr

AZURE DATA ENGINEER (REMOTE) ARC Group has an immediate opportunity for an aspiring Azure / Cloud ... This is a fantastic opportunity to join a well-respected global leader in the supply chain ...

The AI Solutions QA Analyst partners directly with our Analysts and engineering team to ensure ... ships Remote-first, technically rigorous team that takes production quality seriously WHAT YOU'LL ...

Digital Procurement Network, Fresh Solutions, Supply Chain Management, and Software. Buyers Edge ... Collaborate closely with developers on testing results and issues found. About you: * 3+ years ...

Overview Structural Engineer - Buildings - Remote/Hybrid based in Florida (Jacksonville, Orlando ... Their passion for their work clearly shows in the quality of our designs. Here are a few facts ...

Remote Employment Type: Full-Time, Exempt Position Summary The Civil Design Engineer will support ... Attention to detail and commitment to delivering high-quality work. Powered by JazzHR QkqcPy7oj8

next page

Showing results 1-20

Remote Supplier Quality Engineer information

See Boca Raton, FL salary details

$55.5K

$105.8K

$123.4K

How much do remote supplier quality engineer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for remote supplier quality engineer in Boca Raton, FL is $105,785.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $122,400.00 per year, depending on experience, location, and employer.

What is a remote supplier quality engineer?

A Remote Supplier Quality Engineer is responsible for ensuring that a company's suppliers meet quality standards and regulatory requirements while working remotely. They conduct supplier audits, analyze quality data, and collaborate with suppliers to resolve issues. This role often involves virtual assessments, documentation reviews, and communication to maintain product quality and compliance. Strong problem-solving, technical knowledge, and quality management skills are essential.

What are the typical daily responsibilities of a remote supplier quality engineer?

As a Remote Supplier Quality Engineer, your daily tasks often include reviewing supplier quality documentation, analyzing defect data, and coordinating audits or corrective actions with suppliers. You'll regularly communicate with both internal teams and supplier contacts using video calls, emails, and shared project management tools to address quality concerns and ensure compliance with established standards. The role often involves proactively tracking supplier performance metrics, preparing reports, and supporting the resolution of any nonconformities. This position requires a strong sense of organization and the ability to effectively manage priorities across multiple suppliers and projects.

What are the key skills and qualifications needed to thrive in the remote supplier quality engineer position, and why are they important?

A Remote Supplier Quality Engineer should possess a solid background in quality engineering principles, supplier management, and relevant industry standards such as ISO 9001 or IATF 16949, typically supported by a degree in engineering or a related field. Familiarity with tools like SAP, Minitab, and corrective action management systems, as well as certifications like ASQ Certified Quality Engineer, is often preferred. Strong analytical thinking, excellent communication, and the ability to work autonomously in a virtual team environment are key soft skills. These skills ensure effective oversight of supplier performance, timely resolution of quality issues, and successful collaboration with cross-functional teams from a remote setting.

What are the most commonly searched types of Supplier Quality Engineer jobs in Boca Raton, FL? The most popular types of Supplier Quality Engineer jobs in Boca Raton, FL are:
What are popular job titles related to Remote Supplier Quality Engineer jobs in Boca Raton, FL? For Remote Supplier Quality Engineer jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Remote Supplier Quality Engineer jobs in Boca Raton, FL look for? The top searched job categories for Remote Supplier Quality Engineer jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Remote Supplier Quality Engineer jobs? Cities near Boca Raton, FL with the most Remote Supplier Quality Engineer job openings:
Infographic showing various Remote Supplier Quality Engineer job openings in Boca Raton, FL as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $105,785 per year, or $50.9 per hour.

Quality Control Technician (Quality Engineer)

Ubertal Inc

Boca Raton, FL โ€ข Remote

Contractor

Re-posted 18 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.