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Weekend Medical Device Reprocessing Jobs in Wisconsin

Job Title: Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 ... Primarily onsite Monday-Friday, with occasional extended hours, weekends, or holidays to support ...

Manufacturing Engineer

Madison, WI ยท On-site

$73K - $94K/yr

Prior experience in a medical device manufacturing or technical support role is highly desirable ... May require extended hours, weekends, or holidays with manager approval.

No weekend requirements & No call! Why you should become a RN with ThedaCare: * A.D.N to BSN ... Emergency Services/Trauma Care, Obstetrics, Medical Surgical, Intensive Care, Intermediate Care ...

No nights/weekends * No Holidays * PTO & paid anniversary day * 7% GI Associates retirement ... Medical, dental & vision insurance * Flexible spending plan * Short- & long-term disability * Basic ...

No nights/weekends * No Holidays * PTO & paid anniversary day * 7% GI Associates retirement ... Medical, dental & vision insurance * Flexible spending plan * Short- & long-term disability * Basic ...

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Weekend Medical Device Reprocessing information

What are the most commonly searched types of Medical Device Reprocessing jobs in Wisconsin? The most popular types of Medical Device Reprocessing jobs in Wisconsin are:
What cities in Wisconsin are hiring for Weekend Medical Device Reprocessing jobs? Cities in Wisconsin with the most Weekend Medical Device Reprocessing job openings:

Medical Device Quality Engineer

Kellton Tech

Madison, WI โ€ข On-site

$40 - $45/hr

Contractor

Re-posted 7 days ago


Job description

Job Title:ย Medical Deviceย Quality Engineer
Location:ย Madison, WI
Pay Rate : $40--45/hr on W2
Schedule:ย Onsite, Mondayโ€“Friday (standard business hours)

SummaryThe Senior Quality Analyst/Engineer is responsible for ensuring compliance and maintaining strong Quality Systems for the Madison facility. This role oversees CAPA, Change Management, investigations, deviations, Quality Management Reviews, audit coordination, and facility-wide quality metrics. The position supports Quality System improvement initiatives, data trending, reporting, audits, and cross-functional collaboration with Regulatory Affairs, Operations, Technical Operations, Engineering, and Materials Management to strengthen quality culture.

Principal Responsibilities

  • Develop and maintain Quality System processes, including metrics reporting and tracking
  • Manage CAPA initiation, review, surveillance, and reporting
  • Facilitate site Quality Management Reviews
  • Lead and coordinate the site Change Management process
  • Support and lead root cause analysis through cross-functional teams
  • Lead Good Documentation Practice (GDP) training and Quality on the Floor activities
  • Interpret and apply all applicable regulatory requirements
  • Coordinate and support facility audits by internal and external agencies
  • Manage data collection and reporting for product recalls
  • Perform Quality System trending to support FDA and Management reviews
  • Drive quality culture through site initiatives and procedure improvements
  • Review and approve procedures, protocols, and reports as required

Additional/Non-Essential Responsibilities:

  • Documentation filing and management as needed
  • Support other Quality System functions
  • May be required to lead personnel within or outside the Quality organization

Minimum Requirements

Education & Experience:

  • Bachelorโ€™s degree (or higher) in a science or technology field preferred
  • 5+ years of Quality Assurance experience in a cGMP-regulated environment (medical device experience preferred)

Skills & Competencies:

  • Strong communication, coaching/mentoring, and presentation skills
  • Ability to manage change effectively
  • Self-motivated with strong decision-making abilities
  • Project management skills with a track record of on-time delivery
  • Leadership and emotional intelligence
  • Moderate proficiency in statistics for data trending and interpretation

Technical Competencies:

  • Proficient in Microsoft Excel, Word, and PowerPoint
  • Strong technical writing skills
  • Experience with statistical analysis software (e.g., Minitab preferred)

Organizational Relationship / Scope

This role collaborates closely with Manufacturing, Quality Control, Engineering, Facilities, Materials Management, Regulatory Affairs, and Process Development. Must thrive in a fast-paced environment with strict timelines. Primarily onsite Mondayโ€“Friday, with occasional extended hours, weekends, or holidays to support business needs.

Working Conditions

The Senior Quality Analyst will primarily work in an office setting. Limited domestic and international travel may be required.