Medical Device Technician

VIVOS Professional Services, LLC; Madison (WI); On-site; USD 41,328 - 48,216; Full time

Job summary

A medical equipment manufacturing company in Madison, WI is seeking a skilled technician for assembly and testing of medical device products. This full-time position requires a Bachelor’s degree or equivalent experience. The ideal candidate will possess strong problem-solving skills and the ability to work independently while maintaining compliance with quality regulations.

Qualifications

• Ability to work independently and motivate staff to meet required deadlines.
• Experience in cGMP setting and controlled documentation.
• Strong attention to detail while multi-tasking under strict deadlines.

Responsibilities

• Assemble, test, and repair work per established work instructions.
• Perform assembly diagnosis and repair.
• Ensure compliance with EHS and Quality procedures.

Skills

Problem solving

Process improvement

Ability to work independently

Education

Bachelor’s degree in engineering or related scientific field

Associate’s degree with 2+ years’ experience

High School Diploma with 6+ years of experience

Tools

SAP

Job description

Location: Madison, WI (Onsite)

Pay Range: $30-35/hr. on W2 (Rates are comparative)

Scope of Work: Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair, and test equipment maintenance with supervision. Ensure work is completed in compliance with company quality system and medical device regulations.

Essential Functions

• Assemble, test, and repair work per established work instructions, policies and procedures.
• Performs assembly diagnosis and repair.
• Responsible for successful completion of all training in a timely fashion.
• Maintain an organized and professional workspace.
• Notifies area Supervisor and or Team Lead of quality concerns.
• Capability to train other production assemblers as needed.
• Operating within standard operating procedures (SOPs) and assembly drawings.
• Communicate with quality and facilities any time there is an issue with the product or equipment.
• Provide guidance in problem diagnosis and resolution with team members.
• Assist in development and revisions of Standard Operating Procedures (SOP), Work Instructions (WI) device history records, or other quality documentation, as necessary, to support production processes.
• Strong attention to detail, while multi-tasking under strict deadlines.
• Comply with EHS and Quality procedures, regulations and policies.
• Ability to work scheduled or expanded shifts, holidays and/or off-shift duties, as necessary.
• Other duties as assigned.

Education / Experience / Skills

• Bachelor’s degree in engineering or related scientific field. Associate’s degree with 2+ years’ experience or High School Diploma with 6+ years of experience in similar position.
• Ability to work independently and motivate staff to meet required deadlines.
• Problem solving and process improvement skills.

Desired Qualifications

• Experience working in cGMP setting and controlled documentation
• SAP skills and experience.
• Six Sigma belt or LEAN ideology.

Seniority Level

Mid-Senior level

Employment Type

Full-time

Job Function

Manufacturing

Industry

Medical Equipment Manufacturing

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