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Remote Fda Jobs in Illinois (NOW HIRING)

Tempus

Senior Quality Engineer

Chicago, IL · On-site +1

Be involved in the medical device software design controls activities, in accordance with the FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Kasmo Global

Complaint Specialist

Schaumburg, IL · On-site +1

$28/hr

Mon & Fri work remote) (Complaint Specialist) - MDR Remediation Seeking contingent workers to ... Apply current FDA MDR definitions, criteria, and decision trees to legacy complaints to determine ...

Alignerr

Principal Clinical Scientist

Chicago, IL · Remote

This is a fully remote, flexible contract role built for experienced clinical researchers who want ... Evaluate AI-generated clinical analyses for scientific soundness and compliance with FDA, EMA, or ...

Alignerr

Oncology Clinical Researcher

Chicago, IL · Remote

This is a fully remote, flexible contract role. No AI background required - just a strong command ... Translate trial findings into clear regulatory and scientific outputs aligned with FDA, EMA, or ...

Lundbeck

Director US Regulatory Strategy

Deerfield, IL · Remote

$200K - $235K/yr

Remote/Commuter Opportunity - Open to candidates within the United States The Director, US ... Liaises with FDA as needed for all aspects pertaining to drug development, approval, and post ...

Tempus

Lead Quality Engineer

Chicago, IL · On-site +1

$120K - $165K/yr

Responsible for core team oversight of Class 3 US FDA and Class C EU IVDR compliance, including pre ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Tempus

Lead Quality Engineer

Chicago, IL · On-site +1

$120K - $165K/yr

Responsible for core team oversight of Class 3 US FDA and Class C EU IVDR compliance, including pre ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Lundbeck

Director US Regulatory Strategy

Deerfield, IL · Remote

$200K - $235K/yr

Remote/Commuter Opportunity - Open to candidates within the United States The Director, US ... Liaises with FDA as needed for all aspects pertaining to drug development, approval, and post ...

MyMenopauseRx

Physician

Wheaton, IL · On-site +1

... FDA-approved hormone therapy and non-hormonal options, all covered by health insurance. Through ... remote medical team. MyMenopauseRx is an OB/GYN founded and led nationwide medical group and ...

Signature Consultants

Data Entry Clerk

Mundelein, IL · Remote

$17.25 - $23.25/hr

Familiarity with MDR processes, FDA regulations, or quality management systems * Experience working ... Ability to work 40 hours per week with 3 days onsite and 2 days remote * Capability to pass a drug ...

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Remote Fda information

See Illinois salary details

$22.8K

$77.8K

$153.1K

How much do remote fda jobs pay per year?

As of May 28, 2026, the average yearly pay for remote fda in Illinois is $77,781.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,190.00 and $100,910.00 per year, depending on experience, location, and employer.

What is a Remote FDA job?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the key skills and qualifications needed to thrive in the Remote Fda position, and why are they important?

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

What are the typical daily responsibilities of a Remote FDA Compliance Specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.
More about Remote Fda jobs
What are the most commonly searched types of Fda jobs in Illinois? The most popular types of Fda jobs in Illinois are:
What are popular job titles related to Remote Fda jobs in Illinois? For Remote Fda jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Remote Fda jobs in Illinois look for? The top searched job categories for Remote Fda jobs in Illinois are:
What cities in Illinois are hiring for Remote Fda jobs? Cities in Illinois with the most Remote Fda job openings:
Remote Fda jobs near you
Infographic showing various Remote Fda job openings in Illinois as of May 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% Remote job distribution, with an average salary of $77,781 per year, or $37.4 per hour.
Senior Quality Engineer

Senior Quality Engineer

Tempus

Chicago, IL • On-site, Remote

Full-time

Posted 23 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

As a Senior Quality Engineer, you will:

  • Lead verification, validation and maintenance of host systems supporting Tempus Medical Device(s).

  • Lead risk assessments to determine testing strategies.

  • Be involved in the medical device software design controls activities, in accordance with the FDA Quality System Regulation, ISO 13485, GAMP5, Computer System Validation (CSV) standards and FDA guidance, other applicable regulatory requirements, as well as best practices in the software industry.

  • Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and computer systems against user, functional and regulatory requirements.

Responsibilities:

  • Support regulatory compliance of the host system operating with Tempus Medical Device(s).

  • Develop and maintain CSV policies, procedures, templates and work instructions.

  • Lead risk-based approach to host / computer system validation (HSV/CSV), SDLC and design controls activities.

  • Perform validation, re-validation and change controls of various AI, SaaS, and Tempus in-house developed software.

  • Author and review software validation deliverables, including Risk Assessments, Validation Plans, Requirements (URS), Validation Protocols (IQ, OQ, PQ), UAT (User Acceptance Test), and Validation Reports.

  • Collaborate with cross-functional teams in developing test-driven system/functional requirements, defining testing strategies and participating in test execution.

  • Support Change Management and Major Incidents (MI) processes, ensuring organizational compliance and continuous improvement.

  • Provide support to Quality and IT organizations in maintaining compliance to various policies, procedures and activities, including support during internal/external inspections and regulatory and customer audits.

  • Provide CSV guidance, coaching, mentorship, and training to test engineers within the team.

Qualifications

  • BA/B.S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or relevant engineering disciplines.

  • 5+ years experience in FDA regulated domain (e.g. medical device, pharma, biotech)

  • 3+ years experience in Computer System Validation (CSV).

  • Experience with industry standards and best practices for Medical device software and CSV such as Design Controls, GAMP 5, FDA 21 CFR Part 11, FDA (QSR) FDA 21 CFR 820.30, Medical device software (QMS) ISO 13485:2016, FDA 21 CFR 820, and Software life cycle processes (IEC 62304:2006).

  • Knowledge of quality system principles, practices, and standards for the life science industry.

  • Ability to deliver quality outputs without directions or under minimal supervision.

Chicago Pay Range: $90,000-$130,00

NYC/SF Pay Range: $100,000-$150,000

The expected salary range above is applicable if the role is performed from California and may vary for other locations (Colorado, Illinois, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

Additionally,for remote roles open to individuals in unincorporated Los Angeles - including remote roles-Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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