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Manager Arch Medical Solutions Jobs in Racine, WI

Arch Amenities Group

Front Desk/Personal Trainer

Milwaukee, WI · On-site

$13.75 - $17.75/hr

... management entities, bringing together trusted leadership and innovative solutions. Arch Amenities Group proudly operates today with the vision to help maximize the potential of space and the well ...

Arch Amenities Group

Front Desk/Personal Trainer

Milwaukee, WI · On-site

$13.75 - $17.75/hr

... management entities, bringing together trusted leadership and innovative solutions. Arch Amenities Group proudly operates today with the vision to help maximize the potential of space and the well ...

InterSources Inc

Mulesoft Architect

Milwaukee, WI · On-site

Required : • Strong Sol Arch experience in Mulesoft • API Strategies • API Architecture • API Management • Solution Architecture • Integration Arch • Java Full Stack Development Company

Career Site

Front Desk/Personal Trainer

Milwaukee, WI

$13.75 - $17.75/hr

... management entities, bringing together trusted leadership and innovative solutions. Arch Amenities Group proudly operates today with the vision to help maximize the potential of space and the well ...

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All JobsArch Medical Solutions JobsManager Arch Medical Solutions JobsManager Arch Medical Solutions Jobs in Racine, WI

Manager Arch Medical Solutions information

See Racine, WI salary details

$55.8K

$65.6K

$73.6K

How much do manager arch medical solutions jobs pay per year?

As of Sep 8, 2026, the average yearly pay for manager arch medical solutions in Racine, WI is $65,637.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,900.00 and $70,300.00 per year, depending on experience, location, and employer.

What is the difference between Manager Arch Medical Solutions vs Medical Equipment Coordinator?

AspectManager Arch Medical SolutionsMedical Equipment Coordinator
CredentialsBachelor's degree in healthcare administration or related field; management experienceCertification in medical equipment management; technical knowledge
Work EnvironmentHealthcare facilities, administrative officesHospitals, clinics, medical equipment storage areas
Employer & Industry UsageHospitals, healthcare organizations, medical device companiesHospitals, clinics, medical supply companies
Common Search & ComparisonManagement roles in medical solutionsMedical equipment handling and logistics

The Manager Arch Medical Solutions typically oversees medical solution operations, staff, and strategic planning within healthcare organizations. In contrast, the Medical Equipment Coordinator focuses on managing and maintaining medical equipment, ensuring proper functionality and compliance. While both roles require knowledge of medical devices, the manager role emphasizes leadership and administrative duties, whereas the coordinator role is more technical and hands-on.

What are popular job titles related to Manager Arch Medical Solutions jobs in Racine, WI?

For Manager Arch Medical Solutions jobs in Racine, WI, the most frequently searched job titles are:

What job categories do people searching Manager Arch Medical Solutions jobs in Racine, WI look for?

The top searched job categories for Manager Arch Medical Solutions jobs in Racine, WI are:

What cities near Racine, WI are hiring for Manager Arch Medical Solutions jobs?

Cities near Racine, WI with the most Manager Arch Medical Solutions job openings:

Manager Arch Medical Solutions jobs near you
Infographic showing various Manager Arch Medical Solutions job openings in Racine, WI as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $65,637 per year, or $31.6 per hour.

Regulatory Quality Engineer

Kenosha, WI • On-site

Arch-Medical-Solutions
See more jobs at Arch-Medical-Solutionsexternal

$100 - $125/hr

Other

Posted 20 days ago

Job description

  • Acts as a Quality System Management Representative for the Elmhurst (IL) and Kenosha (WI) facilities.
  • Ensures the promotion of awareness of applicable regulatory requirements and quality management system requirements throughout the organization. Assists in training personnel on all aspects of the Quality System and regulatory standards.
  • Ensures that processes needed for the quality management system are established, implemented, and maintained.
  • Complies with all applicable regulatory requirements for medical devices such as FDA Quality System Regulation - 21 CFR 820, GMP guidelines, GDP, ISO 13485, ISO and other applicable regulatory requirements.
  • Leads and/or participates in the development, implementation, compliance, and maintenance of standards (FDA, ISO 13485:2016, etc.) and procedures.
  • Acts as a direct contact for FDA. Ensures FDA registrations and device listings are current.
  • Participates and supports the ECO, CAPA, MRB and other Quality System processes.
  • Creates metrics that drive effective monitoring of processes, value-add improvements and communication at all levels of the organization.
  • Develops and implements process flows in cooperation with functional groups.
  • Ensures risk assessment activities are executed and maintained according to regulatory standards.
  • Organizes investigation activities and coordinates appropriate resources to drive for root cause determinations, correction action implementation and effectiveness verification.
  • Leads vendor, internal/external, and process audits at both facilities and provides necessary documentation.
  • Performs validation training. Establishes and maintains master validation program, including site and individual products and process master validations.
  • Designs and oversees training program(s), including ISO internal training.
  • Responsible for internal and external audits.
  • Interferes with suppliers to resolve quality issues.
  • Coordinates manufacturing process validation requirements, documentation and maintenance of validated processes with internal and external stakeholders.
  • Other duties as assigned.

Qualifications

  • Bachelor's degree in applicable technical discipline such as mechanical or bio-medical engineering is strongly preferred or equivalent,
  • or five to ten years of experience in medical device manufacturing industry and in the quality engineering role, and/or training,
  • or equivalent combination of education and experience.
  • Knowledge of the medical device manufacturing industry.
  • Knowledge of ISO 13485 Quality Management System & FDA 21CFR 820 Regulations.
  • Knowledge of Geometric Dimensioning and Tolerancing per ASME Y14.5M.
  • Familiarity with test methods and standards for the design, verification, and validation of medical device products is required.
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Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

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