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File Transfer Engineer Jobs in Massachusetts (NOW HIRING)

Senior Data Engineer

Waltham, MA · Hybrid

$133K - $156K/yr

Design, develop, and maintain ETL processes using tools like Matillion. Design, Develop and ... Extract data from various sources, such as databases, flat files, and APIs Transform and cleanse ...

Ensure documentation packages are accurate, complete and ready to transfer to suppliers and ... Release technical documentation packages to external vendors and coordinate CAD file conversions

Ensure documentation packages are accurate, complete and ready to transfer to suppliers and ... Release technical documentation packages to external vendors and coordinate CAD file conversions

Data Engineer

Reading, MA · On-site

$120K - $145K/yr

Lead the knowledge transfer and stabilization of existing BigQuery stored procedures, with a ... file-based ingestion methods. * Performance Tuning: Implement table partitioning, clustering, and ...

Data Engineer

North Reading, MA · On-site

$119K - $143K/yr

Lead the knowledge transfer and stabilization of existing BigQuery stored procedures, with a ... file-based ingestion methods. * Performance Tuning: Implement table partitioning, clustering, and ...

Data Engineer

North Reading, MA · On-site

$117K - $140K/yr

Responsibilities : • Lead the knowledge transfer and stabilization of existing BigQuery stored ... file-based ingestion methods. • Implement table partitioning, clustering, and incremental load ...

Senior Systems Engineer

Billerica, MA · On-site

$111K - $151K/yr

Maintain Design History File (DHF) completeness and traceability matrices across hardware, software ... Experience with manufacturing transfer, DFM/DFA, and production readiness reviews for complex ...

Senior Systems Engineer

Billerica, MA · On-site

$125 - $150K/hr

Maintain Design History File (DHF) completeness and traceability matrices across hardware, software ... Experience with manufacturing transfer, DFM/DFA, and production readiness reviews for complex ...

Senior Quality Engineer

Norwood, MA · On-site

$100K - $135K/yr

... transfer, inspection, production, and data monitoring. This role leads quality initiatives and ... Maintain and oversee the Nova Biomedical Validation File and Log (a Microsoft Excel file) and the ...

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File Transfer Engineer information

See Massachusetts salary details

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$19

$25

How much do file transfer engineer jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for file transfer engineer in Massachusetts is $19.37, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $20.72 per hour, depending on experience, location, and employer.

What is the difference between File Transfer Engineer vs Network Engineer?

AspectFile Transfer EngineerNetwork Engineer
CredentialsTypically requires certifications like CompTIA Network+, Cisco CCNA, or similarOften requires Cisco CCNA, CCNP, or equivalent networking certifications
Work EnvironmentFocuses on data transfer protocols, secure file transfer systems, and server configurationsWorks on network infrastructure, routing, switching, and network security
Industry UsageUsed in IT, data management, and enterprise environments handling large data transfersUsed across IT, telecommunications, and enterprise networks

While both roles involve network-related skills, a File Transfer Engineer specializes in managing and optimizing data transfer processes and protocols, whereas a Network Engineer focuses on designing and maintaining overall network infrastructure. The roles often overlap in certifications and work environments, but their core responsibilities differ in scope and focus.

What are File Transfer Engineers?

File Transfer Engineers are IT professionals who specialize in designing, implementing, and managing secure data transfer solutions within and between organizations. They handle protocols such as FTP, SFTP, and managed file transfer (MFT) systems to ensure the reliable and compliant movement of large volumes of data. Their responsibilities often include troubleshooting file transfer issues, automating workflows, and maintaining security standards to protect sensitive information. File Transfer Engineers play a crucial role in supporting business operations that rely on the timely and secure exchange of digital files.

What are the key skills and qualifications needed to thrive as a File Transfer Engineer, and why are they important?

To thrive as a File Transfer Engineer, you need a solid understanding of file transfer protocols (such as SFTP, FTPS, and MFT), networking concepts, and experience with relevant operating systems, often backed by a degree in IT or Computer Science. Familiarity with managed file transfer (MFT) software, automation tools, scripting languages, and sometimes certifications like CompTIA Network+ or vendor-specific credentials are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help you excel in troubleshooting issues and collaborating with stakeholders. These skills ensure secure, reliable, and efficient data transfers critical to business operations and compliance.

What are some common challenges faced by File Transfer Engineers, and how can they be addressed?

File Transfer Engineers often encounter challenges such as managing large volumes of data, ensuring secure and reliable transfers, and troubleshooting failed file transfers. Addressing these issues typically involves implementing robust monitoring tools, establishing clear protocols for error handling, and staying updated with the latest security practices. Collaboration with security, network, and application teams is essential to proactively identify and resolve potential bottlenecks or vulnerabilities, ensuring smooth and compliant file transfer operations.
What are popular job titles related to File Transfer Engineer jobs in Massachusetts? For File Transfer Engineer jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching File Transfer Engineer jobs in Massachusetts look for? The top searched job categories for File Transfer Engineer jobs in Massachusetts are:
What cities in Massachusetts are hiring for File Transfer Engineer jobs? Cities in Massachusetts with the most File Transfer Engineer job openings:
Medical Device Testing Engineer Billerica, MA - Full Time

Medical Device Testing Engineer Billerica, MA - Full Time

GD Resources LLC

Billerica, MA • On-site

$140K - $160K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

Job Title: Senior Design Assurance Quality Engineer
Location: Billerica, MA
Employment Type: Full-Time
Work Arrangement: Onsite
Industry: Medical Devices / Life Sciences / Healthcare Manufacturing
Salary Range: $140,000 - $160,000
Job Summary
Our client is seeking an experienced Senior Design Assurance Quality Engineer to lead Design Assurance and Risk Management activities across innovative medical device product families, including sterile catheter systems, software-enabled products, and electromechanical devices.
This highly collaborative role partners closely with Engineering, Manufacturing, Operations, Regulatory Affairs, Commercial, and Quality teams to ensure products are designed, developed, validated, and transferred into manufacturing in full compliance with FDA regulations, ISO standards, and internal Quality Management System (QMS) requirements. The ideal candidate will serve as the Design Assurance subject matter expert throughout the entire product lifecycle-from concept and development through commercialization and post-market surveillance.
Key Responsibilities
Design Assurance & Product Development
  • Serve as the Design Assurance (DA) Lead on cross-functional product development programs.
  • Ensure compliance with internal Design Control procedures and applicable regulatory requirements throughout the product lifecycle.
  • Guide engineering teams in implementing Design Control and Risk Management best practices.
  • Support all phases of product development, including concept, design, verification, validation, design transfer, and product launch.
  • Review and approve Design Control documentation to ensure regulatory compliance and design integrity.

Risk Management
  • Lead cross-functional Risk Management activities in accordance with ISO 14971.
  • Facilitate:
    • Hazard Analyses
    • Failure Modes and Effects Analyses (FMEA)
    • Risk Management Plans (RMP)
    • Risk Management Reports (RMR)
    • Risk Management Files (RMF)
  • Evaluate product risks and ensure appropriate mitigation strategies are implemented throughout development.

Verification, Validation & Design Transfer
  • Support Design Verification and Validation (V&V) planning and execution.
  • Ensure traceability between design inputs, outputs, verification, validation, and risk controls.
  • Partner with Manufacturing, New Product Introduction (NPI), and R&D teams to ensure successful Design Transfer.
  • Support manufacturing readiness and product commercialization activities.

Software & Product Quality
  • Support software lifecycle quality activities in accordance with IEC 62304.
  • Participate in product cybersecurity initiatives.
  • Ensure software quality processes align with regulatory and company standards.

Quality Engineering & Continuous Improvement
  • Serve as a subject matter expert for:
    • Statistical Analysis
    • Root Cause Analysis (RCA)
    • Failure Investigations
    • Risk Assessments
  • Support Post-Market Surveillance (PMS) activities.
  • Collaborate with third-party suppliers and vendors to ensure quality and compliance.
  • Drive continuous improvement initiatives that strengthen product quality and regulatory compliance.

Required Qualifications
  • Bachelor's Degree in Engineering or a related technical discipline.
  • Minimum 5-8 years of Design Assurance or Quality Engineering experience within the medical device or life sciences industry.
  • Experience supporting New Product Introduction (NPI) and Design Transfer.
  • Strong working knowledge of:
    • FDA 21 CFR Part 820
    • ISO 13485
    • ISO 14971:2019
  • Experience supporting Design Controls throughout the complete product development lifecycle.
  • Experience managing risk management activities and quality documentation.
  • Strong communication, collaboration, and project leadership skills.

Preferred Qualifications
  • Experience with:
    • IEC 62304 (Medical Device Software)
    • IEC 60601 (Medical Electrical Equipment)
    • ISO 10993 (Biocompatibility)
  • Experience supporting regulatory submissions and documentation.
  • Experience managing third-party suppliers and contract manufacturers.
  • Experience working in highly regulated medical device manufacturing environments.

Technical Skills
Candidates should possess expertise in:
Quality & Regulatory
  • FDA 21 CFR Part 820
  • ISO 13485
  • ISO 14971:2019
  • Design Controls
  • Risk Management
  • Design Assurance
  • Product Lifecycle Management
  • Regulatory Documentation
  • Post-Market Surveillance

Risk & Quality Engineering
  • FMEA
  • Hazard Analysis
  • Root Cause Analysis (RCA)
  • Statistical Process Control (SPC)
  • Measurement Systems Analysis (MSA)
  • Gage R&R
  • Failure Investigations
  • Corrective & Preventive Actions (CAPA)

Validation & Product Development
  • Design Verification
  • Design Validation
  • IQ/OQ/PQ Validation
  • Design Transfer
  • New Product Introduction (NPI)

Software & Data Analysis
  • Minitab
  • Statistical Analysis
  • Microsoft Office Suite
  • Medical Device Software Quality (IEC 62304)
  • Product Cybersecurity

Leadership & Professional Skills
  • Proven ability to lead cross-functional project teams through influence.
  • Strong organizational and project management skills.
  • Excellent analytical and critical thinking abilities.
  • Exceptional written and verbal communication skills.
  • Ability to manage multiple priorities in a fast-paced product development environment.
  • Self-motivated with a continuous improvement mindset.
  • Strong interpersonal skills with the ability to build collaborative relationships across engineering, manufacturing, quality, and regulatory teams.

Working Conditions
  • Primarily office environment with regular interaction in engineering laboratories and manufacturing facilities.
  • Occasional work within controlled production environments requiring appropriate Personal Protective Equipment (PPE).
  • Minimal travel may be required to support suppliers, manufacturing sites, or customer activities.

Why Join Our Client?
  • Lead Design Assurance activities for innovative next-generation medical device technologies.
  • Work with cross-functional teams developing products that improve patient outcomes worldwide.
  • Join a collaborative, quality-driven engineering organization focused on innovation and regulatory excellence.
  • Competitive compensation package with salaries ranging from $140,000-$160,000.
  • Opportunity to influence product quality from concept through commercialization and post-market support.
  • Career growth within a dynamic and rapidly evolving medical device environment.