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 Quality Control Inspector

Details
Country: USA
Location: Franksville WI
Total applied: 40
Location:US-WI-Franksville

Base Pay:N/A
Employee Type:Full-Time Employee

Industry:Manufacturing Medical Equipment

Manages Others:no
Quality Control Inspector

Position Summary:
Support the day-to-day testing and inspection requirements for the production of BioForm and OEM product. Perform and/or assist with tasks associated with the inspection and/or testing of components, subassemblies and finished goods. Assist with other tasks as assigned related to the activities associated with operation of BioForm’s Quality System.

Essential Duties and Responsibilities:
Learn and perform Quality tests and inspections required to manufacture product.
Learn and support other Quality System functions as assigned that may be related to documentation review, equipment calibration, Non-conformance review, Corrective and Preventative Actions, First Article Inspections and other tasks as directed.
Learn, understand, and promote the use of the Quality System Standards, Quality System Regulations, and other company procedures around which the Quality System is developed.
Test and/or inspect Incoming materials, and In-Process and Finished Product.
Assist with the calibration of equipment.
Perform First Article Inspections (F.A.I.R.) as required.
Assist with the preparation of product labels.
Support the work associated with studies related to sterilization, evaluation of new materials or other quality assurance, manufacturing and/or R & D type projects.
Assist other Quality Assurance personnel as required.

Position Requirements and Competency Measurements
Education and/or Experience (years):
Minimum High School Diploma or equivalent.
Familiar with basic Quality Control Inspection methods and procedures.
Familiar with clean room operating procedures.
Minimum 1 year experience in the medical device field or other Quality Control/Quality Assurance trade.

Knowledge, Skills and Abilities:
Familiar with incoming, in process and final product testing procedures.
Familiar with the use of basic measurement and lab equipment. Familiar with ISO 9000/ISO 13485 Quality System Standards, FDA Quality System Regulations, GMP’s and/or other international medical device regulations desirable.
Basic computer skills including those associated with word processing, spread sheet programs and data bases.
Ability to work with little or no supervision.

This position will start on 1st shift with the potential to move to 2nd shift once trained.

Interested candidates in Wisconsin and northern Illinois please respond via e-mail.
REQUIREMENTS
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