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60 Cms Jobs Hiring in Wisconsin

Lund Boats

Web Content Specialist

Menomonee Falls, WI · On-site

CMS Content Operations * Execute content publishing, updates, and configuration changes across multiple brand websites using enterprise CMS platforms (AEM, Optimizely, or equivalent). * Build and ...

Brunswick

Web Content Specialist

Menomonee Falls, WI · On-site

CMS Content Operations * Execute content publishing, updates, and configuration changes across multiple brand websites using enterprise CMS platforms (AEM, Optimizely, or equivalent). * Build and ...

RIT Solutions

Frontend Developer

Madison, WI · Remote

$103K - $120K/yr

Integrate frontend components with a headless CMS (Sitecore) and backend APIs * Collaborate with design and product teams to translate requirements into high-quality user experiences * Develop ...

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Kentico Developer

Waukesha, WI · On-site

Kentico developer Duration: 3 months contract to hire Responsible for the hands-on, front-end development of websites using Kentico CMS on behalf of the Digital Marketing team. Collaborate with IT to ...

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Regulatory & Quality Assurance Specialist (DME/CMS Compliance)

Astrix Inc

New Berlin, WI • On-site

$68K - $83K/yr

Full-time

Re-posted 7 days ago

Job description

Pay Rate Low: 68000 | Pay Rate High: 83000
Our client is a well-established global healthcare company focused on designing and manufacturing specialized medical devices for airway management, speech rehabilitation, and respiratory care.
Title: Regulatory & Quality Assurance Specialist (DME/CMS Compliance)
Location: New Berlin, WI
Schedule: 100% Onsite, Monday-Friday, 8:00 AM-5:00 PM)
Pay: $68,000-$83,000 +Annual Bonus (Based on experience level)
We are seeking a Regulatory & Quality Assurance Specialist to support regulatory compliance, quality systems, accreditation, and audit readiness for a growing Durable Medical Equipment (DME) business. This position is ideal for candidates with DMEPOS, CMS (Medicare/Medicaid), healthcare compliance, or accreditation audit experience. Candidates whose background is primarily in manufacturing QA may not be the best fit, as this role focuses on commercial healthcare regulatory compliance rather than manufacturing quality.
Key Responsibilities:
  • Manage regulatory compliance documentation and maintain audit-ready records.
  • Support DMEPOS accreditation applications, renewals, and CMS site visits.
  • Coordinate and prepare for CMS, accreditation, and external audits.
  • Maintain Quality Management System (QMS) documentation, SOPs, policies, and document control.
  • Assist with CAPA, non-conformance investigations, change controls, and internal audits.
  • Support transparency reporting and regulatory reporting requirements.
  • Partner with Legal, Compliance, and cross-functional teams to ensure compliance with FDA, HIPAA, Medicare/Medicaid, and state regulations.

Required Qualifications:
  • 3-5 years of Regulatory Affairs, Quality Assurance, or Compliance experience in the healthcare industry.
  • Experience with DMEPOS, CMS (Medicare/Medicaid), healthcare audits, accreditation, or regulatory compliance.
  • Working knowledge of Quality Management Systems (QMS) and U.S. healthcare regulations.
  • Experience supporting audits, documentation, CAPA, SOPs, and compliance reporting.
  • Strong organizational, analytical, and communication skills.
  • Proficiency with Microsoft Office; Brightree, SAP, and Salesforce are a plus.
  • Bachelor's degree preferred (High School Diploma/GED with relevant experience considered).

Preferred Experience:
  • Durable Medical Equipment (DME) industry experience.
  • CMS or Medicare/Medicaid audit preparation.
  • Accreditation readiness and site visit coordination.
  • Process improvement and project management experience.
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