Compliance Analyst, IT/Tech
Job in
Chicago, Cook County, Illinois, 60601, USA
Listed on 2026-07-18
Listing for:
Hired by Matrix
Full Time
position Listed on 2026-07-18
Job specializations:
-
IT/Tech
-
Quality Assurance - QA/QC
Job Description & How to Apply Below
Compliance Analyst
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company? If so, our client is hiring a Compliance Analyst. Position Type:
Contract, Remote.
This role is fully remote, but candidates must be able to align with US Central Time working hours, ideally 8:00 AM to 5:00 PM CT.
Required:
- Bachelor's degree in engineering or related technical field (or equivalent technical certification of ≥350 hours).
- Experience in medical device labeling, packaging documentation, quality documentation, regulatory documentation, or document control.
- Strong understanding of controlled document environments and regulated medical device workflows.
- Experience reviewing and updating IFUs, packaging labels, product files, or related labeling documentation.
- Excellent attention to detail and ability to work through large volumes of repetitive documentation accurately.
- Ability to follow an approved naming convention and apply it consistently across documentation.
- Strong organizational skills and ability to track multiple documents, products, and updates simultaneously.
- Ability to work remotely while aligning with U.S. Central Time business hours.
- Strong written communication skills and ability to document findings clearly.
Preferred:
- Experience supporting EU MDR-related remediation, technical documentation updates, or legacy product remediation.
- Prior experience with Smart Solve and/or IQVIA.
- Experience with labeling change control, packaging artwork updates, or document management systems.
- Background in cardiovascular, implantable, or complex medical devices is a plus.
- Experience supporting product launch readiness or post-approval remediation activities.
Responsibilities:
- Review labeling-related documentation for approximately 22 legacy medical device products, including packaging labels, IFUs, and related product files.
- Perform a detailed gap assessment to identify inconsistencies in product naming across controlled documentation.
- Document required labeling and packaging updates based on the approved naming convention provided by the client.
- Support execution of approved updates to labeling, packaging documentation, and related controlled files.
- Work within established document control and change control processes.
- Track progress across a high volume of documents and ensure updates are completed accurately and consistently.
- Collaborate with client stakeholders to clarify documentation requirements, priorities, and review expectations.
- Maintain organized records of reviewed documents, identified gaps, required actions, and completed updates.
- Support readiness for market launch by helping ensure naming consistency across impacted labeling documentation.
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