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Freelance Quality Engineer Fda Jobs in Springfield, MA

medplast

Senior Toolmaker

Brimfield, MA · On-site

$32 - $41/hr

Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug ... FDA) regulations, Company policies and operating procedures, and other regulatory requirements. • ...

medplast

Senior Toolmaker

Brimfield, MA · On-site

$32 - $41/hr

Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug ... FDA) regulations, Company policies and operating procedures, and other regulatory requirements. • ...

medplast

Senior Toolmaker

Brimfield, MA · On-site

$32 - $41/hr

Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug ... FDA) regulations, Company policies and operating procedures, and other regulatory requirements. • ...

Cirtec Medical Corp.

Sr. Project Manager

Enfield, CT

Facilitate collaboration across engineering, quality, operations, and other functional teams to ... Must possess strong understanding and working knowledge of ISO 13485 and FDA 21CFR820 based Quality ...

Viant

Senior Toolmaker

Brimfield, MA · On-site

$32 - $41/hr

Quality Management Systems (QMS), Environmental Management Systems (EMS), U.S. Food and Drug ... FDA) regulations, Company policies and operating procedures, and other regulatory requirements. • ...

florrent

Laboratory Manager

Northampton, MA

... looking for scientists and engineers passionate about solving hard problems and delivering ... This role is critical to maintaining our high standards of quality, safety, and efficiency as we ...

medplast

Director of Operations

Brimfield, MA · On-site

$180 - $210K/hr

... Quality, Supply Chain, Sales) * Oversees and manages the activities of: production, engineering ... Knowledge of FDA GMP, ISO 13485, and regulatory requirements * Six Sigma Green/Black Belt and/or ...

medplast

Director of Operations

Brimfield, MA · On-site

$180 - $210K/hr

... Quality, Supply Chain, Sales) * Oversees and manages the activities of: production, engineering ... Knowledge of FDA GMP, ISO 13485, and regulatory requirements * Six Sigma Green/Black Belt and/or ...

medplast

Director of Operations

Brimfield, MA · On-site

$180 - $210K/hr

... Quality, Supply Chain, Sales) * Oversees and manages the activities of: production, engineering ... Knowledge of FDA GMP, ISO 13485, and regulatory requirements * Six Sigma Green/Black Belt and/or ...

Viant

Director of Operations

Brimfield, MA · On-site

$180 - $210K/hr

... Quality, Supply Chain, Sales) * Oversees and manages the activities of: production, engineering ... Knowledge of FDA GMP, ISO 13485, and regulatory requirements * Six Sigma Green/Black Belt and/or ...

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All JobsQuality Engineer Fda JobsFreelance Quality Engineer Fda JobsFreelance Quality Engineer Fda Jobs in Springfield, MA

Freelance Quality Engineer Fda information

See Springfield, MA salary details

$44.8K

$83.7K

$118.6K

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

As of Aug 13, 2026, the average yearly pay for freelance quality engineer fda in Springfield, MA is $83,745.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,700.00 and $92,700.00 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?

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.
What are popular job titles related to Freelance Quality Engineer Fda jobs in Springfield, MA? For Freelance Quality Engineer Fda jobs in Springfield, MA, the most frequently searched job titles are:
What job categories do people searching Freelance Quality Engineer Fda jobs in Springfield, MA look for? The top searched job categories for Freelance Quality Engineer Fda jobs in Springfield, MA are:
What cities near Springfield, MA are hiring for Freelance Quality Engineer Fda jobs? Cities near Springfield, MA with the most Freelance Quality Engineer Fda job openings:
Freelance Quality Engineer Fda jobs near you

Looking for Senior Project Engineer @ East Hartford, Connecticut Onsite

Lorven Technologies

East Hartford, CT • On-site

$97K - $127K/yr

Full-time

Re-posted 11 days ago

Job description

Mandatory Qualifications:
• Bachelor's degree in Engineering (Mechanical, Electrical, Industrial, Systems, or related field)
• 5+ years of experience in a Project Engineer, Engineering Project Manager, or similar technical coordination role. Aerospace domain experience is required.
• Proven ability to organize and manage technical data across multiple projects
• Strong experience aligning schedules and coordinating tasks across cross functional engineering teams
• Demonstrated ability to drive cross functional teams and influence without direct authority
• Excellent written and verbal communication skills
• Proficiency with project tracking tools (e.g., MS Project, Smartsheet, Jira, or similar) and Microsoft Office
• Outstanding analytical and problem solving skills
• Outstanding communication and interpersonal skills
• Outstanding customer interfacing skills
• Demonstrated leadership abilities
• Must be a U.S. Citizen
Preferred Qualifications
• Proven experience in engineering project management, preferably in a regulated industry such as aerospace
• Project Management Professional (PMP) certification is a plus
• Schedule driven mindset with attention to detail
• Ability to balance technical depth with project execution
• Comfortable managing multiple priorities in a fast-paced environment
• Collaborative, proactive, and solution oriented
• Knowledge of regulatory standards such as ISO 9001, AS9100, or FDA regulations
• An understanding of engineering outsourcing business practices
• Experience writing or creating standard work, establishing processes, and documenting lessons learned
• An alignment with LTTS company values, including: Being Purposeful, Ethics & Integrity, Caring, A Culture of Learning, and Results with Accountability.
Physical Requirements:
• Prolonged periods sitting at a desk and working on a computer
• Ability to traverse and navigate a manufacturing facility
• Must be able to lift up to 15 pounds at times
Qualification:
• Bachelor's degree in engineering (Mechanical, Electrical, Industrial, Systems, or related
field) or Aerospace Engineering. PMP Certification Preferred
Primary Responsibilities
• Organize, track, and maintain technical data, including requirements, specifications, drawings, change documentation, and project deliverables
• Develop, maintain, and align project schedules, milestones, and dependencies across multiple engineering disciplines
• Drive cross functional teams to ensure timely execution of engineering tasks and resolution of technical issues
• Act as the primary technical point of contact between engineering, manufacturing, quality, and program stakeholders
• Support project planning, risk identification, and mitigation activities
• Coordinate design reviews, technical reviews, and project status meetings
• Track action items, technical decisions, and deliverables to closure
• Support configuration management and change control processes
• Prepare and present clear project status updates to leadership and stakeholders
• Update status reports, present project status to customers, and work with LTTS project management to ensure productive and consistent customer communication.
• Understand and adhere to all export control regulations.
• Travel locally onsite to the customer facility several days per week as needed, and comply with all customer site requirements.
This is considered an onsite working position, meaning this role will require working from our office in Hartford, and/or the customer facility in East Hartford, Connecticut daily. There is potential for a hybrid working arrangement but is not guaranteed with this position.
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About Lorven technologies

Sourced by ZipRecruiter

Lorven Technologies, headquartered in Plainsboro, New Jersey, United States, is a reputable company in the technology industry, specializing in providing effective IT solutions and consulting services. The company's official website, lorventech.com, offers comprehensive insights into its offerings which include but are not limited to software development, IT consulting, project management, and business analysis. Since its inception, Lorven Technologies has been committed to ensuring efficiency and reliability in delivering IT services to its global clientele, establishing itself as a trusted name in the industry.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Plainsboro, NJ, US

Year founded

2001

Social media

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