Medical Device Technician

Job Title: Medical Device Technician

Job Location: Madison WI 53718 (Onsite

Job Duration: 6 Month contract with possible extension or conversion

Timings: 0600 and 0730 CST. Working 9 hr days Mon-Thur. 4hr on Fri

Job Description:

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.

Minimum Requirements
Education / Experience / Skills:
Bachelors degree in engineering or related scientific field. Associates 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