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File Transfer Engineer Jobs in Chicago, IL (NOW HIRING)

Intellectt INC

Quality Engineer

Chicago, IL · On-site

$74K - $95K/yr

Help with design planning, design inputs/outputs, verification, validation, and product transfer ... Maintain quality documents like DHF, risk files, design reviews, and traceability matrices. * Work ...

Arka Infotech Inc

3PAR Engineer

Franklin Park, IL · On-site

$79K - $107K/yr

... other file copy/movement/management as necessary o Daily analysis of SAN utilization and disk ... transfer with the goal of full adoption by Client Operations within allotted timeframe.

CYNET SYSTEMS

Sustaining Quality Engineer

Naperville, IL · On-site

$40 - $45/hr

Collaborate with engineering teams to ensure successful transfers. * May develop, update, and maintain technical content of risk management files, review and revise pFMEAs in conjunction with BU PMS ...

Seko Logistics

Security Analyst

Schaumburg, IL · Hybrid

$70K - $100K/yr

Monitor regulatory changes affecting data privacy Security Architecture & Engineering * Help ... Familiarity with application security, API security, and secure file transfer protocols

Seko Logistics

Security Analyst

Schaumburg, IL · On-site

$70K - $100K/yr

Monitor regulatory changes affecting data privacy Security Architecture & Engineering * Help ... Familiarity with application security, API security, and secure file transfer protocols

TalentBurst, Inc.

Quality Engineer II

Naperville, IL · On-site

$71K - $92K/yr

Collaborate with engineering teams to ensure successful transfers * May develop, update, and maintain technical content of risk management files, review and revise pFMEAs in conjunction with BU PMS ...

SunCoke Energy

Engineer - Maintenance

East Chicago, IN · On-site

Experience with materials handling, heat transfer systems, boiler systems, flue gas desulfurization ... Knowledge of computer operating systems, file management, email and basic programs. * Time and ...

AgileEngine

Senior Data Engineer ID75059

Berwyn, IL · On-site +1

$107K - $146K/yr

You will implement Python-based ETL/ELT pipelines, orchestrate workflows with Airflow, develop ... file formats (Parquet, Avro, ORC) and columnar storage to ensure high-performance data retrieval ...

SunCoke Energy

Engineer - Maintenance

East Chicago, IN · On-site

Experience with materials handling, heat transfer systems, boiler systems, flue gas desulfurization ... Knowledge of computer operating systems, file management, email and basic programs. * Time and ...

Tredence Analytic

Data Engineer

Chicago, IL

$118K - $141K/yr

... file using efficient programming processes. * Write and refine code to ensure performance and ... in ETL development. * Collaborate with Quality Assurance resources to debug code and ensure the ...

Tata Consultancy Service Limited

ETL Lead

Lisle, IL · On-site

$90K - $120K/yr

Understanding on different Snowflake functionalities like File Stage, Tasks, etc. • Good communication, and documentation skills • Experienced in working in a customer facing role • Experience ...

Tata Consultancy Service Limited

ETL Lead

Lisle, IL · On-site

$90K - $120K/yr

Understanding on different Snowflake functionalities like File Stage, Tasks, etc. • Good communication, and documentation skills • Experienced in working in a customer facing role • Experience ...

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All JobsFile Transfer Engineer JobsFile Transfer Engineer Jobs in Chicago, IL

File Transfer Engineer information

See Chicago, IL salary details

$12

$18

$24

How much do file transfer engineer jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for file transfer engineer in Chicago, IL is $18.30, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $19.57 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 Chicago, IL? For File Transfer Engineer jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching File Transfer Engineer jobs in Chicago, IL look for? The top searched job categories for File Transfer Engineer jobs in Chicago, IL are:
File Transfer Engineer jobs near you
Infographic showing various File Transfer Engineer job openings in Chicago, IL as of July 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $38,056 per year, or $18.3 per hour.
Sr. Design Quality Engineer

Sr. Design Quality Engineer

Avalign Technologies

Schaumburg, IL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Avalign Technologies rating

8.3

Company rating: 8.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

Job description

Avalign produces innovative, high-performance, and cost-effective medical devices with a particular focus on high growth and ingenuity. Our team is growing quickly and proud of the fact that our custom-made devices continue to make a huge difference in the lives of medical professionals and their patients. Our employees are actively involved in the design, engineering and manufacture of technologically advanced medical devices that ensure that we meet our customer's quality specifications for each product we produce.
The Design Quality Engineer will be responsible for the quality and regulatory related activities associated with new product development. New product development activities will occur in the contract development context and in the specification developer context. These activities span all aspects of the new product development process. The Design Quality Engineer will advise customers in the contract development context how to incorporate Critical-To-Quality (CTQ) and Design-For-Inspection (DFI) into the development process. The Design Quality Engineer will provide CTQ and DFI input internally while ensuring that Avalign specification development activities conducted by Research and Development (R&D) comply with associated policies, procedures and work instructions as outlined in the design control elements of the Quality Management System (QMS).
The Design Quality Engineer will be responsible to ensure that regulatory compliant technical documentation is compiled and for ensuring the ongoing compliance of the technical documentation for assigned Avalign Technologies design owned products. The Design Quality Engineer will assist in regulatory filings for Avalign Technologies design owned products whether this includes Avalign filing, supporting the customer to file, or a third party filing the regulatory submission.
A working knowledge of related global design regulations is required. (ISO 13485, ISO 14971, 21 CFR Part 820, and, preferably, EU Medical Device Regulation) The position requires a hands-on self-directed style, and the ability to influence and effectively communicate vertically, horizontally, across functions, externally with customers and internally with co-workers. The ideal candidate must demonstrate ability to self-direct, strong analytical abilities, and strong verbal and written communication skills. The position reports directly to the Director of Regulatory Affairs.
What You Will Do:
  • Responsible for supporting a design control quality system that is complaint to ISO 13485 (latest revision), the Medical Device Directives (while active), and the EU Medical Device Regulations (MDR).
  • Supports, reviews, and approves the following activities associated with new product development: identification and documentation of user needs, design inputs, outputs, verification, validation, risk assessment, and design change activities to demonstrate new product designs are supported by objective evidence in the design history file prior to product launch.
  • Participate in supply chain development through Avalign division and external supplier selection and qualification with the new product development team.
  • Participates in design reviews as required by the design control and development processes.
  • Serve as GD&T expert for contract developer and specification developer activities.
  • Assist project managers with design transfer planning and execution including advising on Avalign and vendor manufacturing process validations to support new product development.
  • Support processes for Medical Device Reporting and Complaints for Avalign as specification developer products.
  • Ensure required design documentation is retained in design history files and technical files to support regulatory submissions and audits.
  • Support and maintain all regulatory filings for all Avalign Technologies design owned products whether this includes Avalign filing, supporting the customer to file, or a third party filing the regulatory submission.
  • Perform corporate internal audits, either as a supporting auditor or as the lead auditor.
  • Participate in external audits.
  • Conduct post market surveillance for contract development and specification developer products.
  • Ensure post launch product design file updates are completed following design change and post market surveillance activities.
  • Write or update standard operating procedures, work instructions, or policies.
  • Prepare responses to customer requests for information, such as product data, written regulatory affairs statements, surveys, or questionnaires.
  • Assist in investigations of product complaints, root cause analysis, corrective action, trending and make recommendations regarding their reportability.
  • Investigate and complete records related to assigned Nonconformances and CAPAs.
  • Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or other compliance issues.

What You Will Need:
  • Bachelor degree or equivalent experience in an engineering or scientific field
  • 5+ years of experience in quality and/or engineering role
  • 2+ years of experience in medical device industry, preferred
  • 2+ years of experience in quality within design control activities supporting new product development, preferred
  • Experience with ISO 13485, FDA 21 CFR 820 Quality System Regulation, ISO 14971, MDR, or associated regulations.
  • Ability to travel up to 25%

Preferred Qualifications
  • Expertise in project management and problem solving skills, including the ability to identify, investigate and resolve technical and/or systemic issues.
  • High attention to detail and persistence in resolving discrepancies
  • Excellent interpersonal communication (written and verbal) skills and ability to communicate at all levels of the organization and with suppliers and customers
  • Familiarity with Quality System Management software
  • Familiarity with regulatory submissions including:
    • Coordinating efforts associated with the preparation of regulatory documents or submissions.
    • Preparation or review of regulatory submissions for domestic or international projects.

What You Won't Do:
  • Feel stuck - we offer great opportunities to advance and learn
  • Get bored - we make a high variety of products, so no day is the same
  • Feel like a number - we're a close-knit bunch and always have each other's backs

Who You Are:
  • A self-starter who thrives in a fast-paced environment
  • A quick learner who is always ready to gain depth of knowledge in manufacturing processes
  • A reliable individual who knows the importance of showing up when it counts
  • Someone who accept assignments with an open, cooperative, positive and team-oriented approach
  • Someone who is able to plan and execute plans across teams
  • An effective communicator, both written and verbal

What You'll Enjoy:
  • Competitive compensation and benefits package
  • Comprehensive medical, dental, and vision insurance
  • Paid vacation and 10 observed paid holidays per year
  • Employer funded Basic Life and AD&D insurance
  • Employer funded STD and LTD insurance
  • Tuition reimbursement
  • Great 401(k) with company match
  • Generous employee referral bonus program
  • Working for a thriving, performance-based company that values promoting from within and career advancement
  • Temperature controlled environment
  • Community involvement investing and giving back to the community
  • Additional free resources such as travel assistance, EAP, etc.

Avalign conducts a comprehensive background, drug testing, highest level of education completion verification, and reference checks.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, national origin, gender identity, sexual orientation, age, marital status, veteran status, or disability status. We are an employer that participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

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