Energy Jobline ZR
Medical Device Quality Inspector
Location:
Femrite Drive, Madison, WI 53718
Pay Rate:
$25/hr on w2
Contract Duration:
6 months
Responsibilities
Ensure materials, activities, processes, and specified conditions related to daily device manufacturing, processing, and packaging meet current GMP standards and comply with applicable procedures and standards.
Ensure work is completed in compliance with the company quality system and medical device regulations.
Perform one of three functions in the Quality department:
Inspect raw materials to meet production requirements.
Conduct in‑process inspection of manufacturing product and processes.
Review final documentation and shipment packaging for medical devices, subassemblies, and kits.
Assist in the Madison Manufacturing documentation control room.
Complete documentation of activities performed, prepare and attach material quality status labeling, and ensure storage and handling of product and labeling in a controlled and secure manner.
Support Quality through occasional conduct of investigations of nonconformance, assist with preventive actions associated with the QA unit.
Perform quality reviews for quarantine releases on non‑reportable, non‑complaint, RMF‑3 internal to an RSC.
Education / Experience / Skills
High School diploma or equivalent.
One year’s experience in a regulated work environment.
Knowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing.
Competencies
High level of motivation; ability to work independently.
Detail oriented.
Ability to work with computer‑based systems daily.
Collaborator with strong engagement with individuals and as a team member.
Good interpersonal skills; ability to communicate well, both verbally and written.
Organizational Relationship/Scope Reports to the Quality Control Manager. This position is accountable for delivery of prompt investigative work and detailed reporting. Working across multiple functions, this position collaborates primarily with manufacturing, engineering, and quality to assess nonconforming product and support supplier quality issues.
Working Conditions Manufacturing facility of medical devices and accessories. Controlled environmental working conditions.
Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr
Femrite Drive, Madison, WI 53718
Pay Rate:
$25/hr on w2
Contract Duration:
6 months
Responsibilities
Ensure materials, activities, processes, and specified conditions related to daily device manufacturing, processing, and packaging meet current GMP standards and comply with applicable procedures and standards.
Ensure work is completed in compliance with the company quality system and medical device regulations.
Perform one of three functions in the Quality department:
Inspect raw materials to meet production requirements.
Conduct in‑process inspection of manufacturing product and processes.
Review final documentation and shipment packaging for medical devices, subassemblies, and kits.
Assist in the Madison Manufacturing documentation control room.
Complete documentation of activities performed, prepare and attach material quality status labeling, and ensure storage and handling of product and labeling in a controlled and secure manner.
Support Quality through occasional conduct of investigations of nonconformance, assist with preventive actions associated with the QA unit.
Perform quality reviews for quarantine releases on non‑reportable, non‑complaint, RMF‑3 internal to an RSC.
Education / Experience / Skills
High School diploma or equivalent.
One year’s experience in a regulated work environment.
Knowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing.
Competencies
High level of motivation; ability to work independently.
Detail oriented.
Ability to work with computer‑based systems daily.
Collaborator with strong engagement with individuals and as a team member.
Good interpersonal skills; ability to communicate well, both verbally and written.
Organizational Relationship/Scope Reports to the Quality Control Manager. This position is accountable for delivery of prompt investigative work and detailed reporting. Working across multiple functions, this position collaborates primarily with manufacturing, engineering, and quality to assess nonconforming product and support supplier quality issues.
Working Conditions Manufacturing facility of medical devices and accessories. Controlled environmental working conditions.
Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr