What are the responsibilities and job description for the Medical Device Quality Inspector - Madison, WI position at Lenmar Consulting Inc?
Title: Medical Device Quality Inspector
Location: Madison, WI
Duration: 6 months contract with extension up to 18 months and possible fulltime conversion
Pay rate range: $28/hr-$30/hr
Responsible for assuring that materials, activities, processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP standards and comply with applicable procedures and standards such as ensuring the quality integrity of the product. Ensure work is completed in compliance with the company quality system and medical device regulations. Ensure work is completed in compliance with the company quality system and medical device regulations.
Essential Functions
Education / Experience / Skills:
Manufacturing facility of medical devices and accessories. Controlled environmental working conditions.
Location: Madison, WI
Duration: 6 months contract with extension up to 18 months and possible fulltime conversion
Pay rate range: $28/hr-$30/hr
Responsible for assuring that materials, activities, processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP standards and comply with applicable procedures and standards such as ensuring the quality integrity of the product. Ensure work is completed in compliance with the company quality system and medical device regulations. Ensure work is completed in compliance with the company quality system and medical device regulations.
Essential Functions
- Performs one of three functions in the Quality department:
- Inspecting raw materials to meet production requirements
- Conducts in-process inspection of manufacturing product and processes
- Reviews final documentation and shipment packaging for medical devices, subassemblies, and kits
- Assists in the Madison Manufacturing documentation control room.
- Completes documentation of activities performed, prepares and attaches material quality status labeling. Ensures storage and handling of product and labeling in a controlled and secure manner.
- Supports Quality through occasional conduct of investigations of nonconformance, assists with preventive actions associated with the QA unit.
- Performs 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 preferred
- Knowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing
- High Level of motivation; ability to work independently
- Detailed oriented
- Ability to work with computer-based systems daily
- Collaborator with strong levels of engagement with individuals and as a team member
- Good interpersonal skills; ability to communicate well, both verbally and written
Manufacturing facility of medical devices and accessories. Controlled environmental working conditions.
Salary : $28 - $30