QA Final Inspector

United States of America, Wisconsin, MadisonR
5027648

United States of America Quality and Regulatory Affairs Job description

The QA Final Inspector is responsible for performing assessments, validation and measurement of loupes, in process and in final form. This critical position determines whether the medical device is compliant with quality and functional requirements and was successfully and accurately manufactured to the specific customer measurements. The QA Final Inspector oversees documentation of final product inspection and keeps Production and QA management informed of state of finished loupe quality ential Duties and Responsibilities Perform quality checks on in-process and finished devices, as assigned, completing and documenting all SOP quality inspection requirements

Perform reviews of completed work orders for accuracy and completeness

Complete all visual and measurement tests associated with each product, per specifications

Based on quality assessment and inspection, determine final acceptance of product, or return to production for re-work Document inspection outcomes in accordance with the SOP instructions, including date and signature

Use Master Control to store completed work orders/device history records

Provide Production and QA Management with all products final inspection outcomes. Develop and generate daily, weekly and monthly reports on outcomes, including trend analysis

Maintain all related quality inspection records

Keep track of the Data and enter them in to excel sheet and Visual Management Board.

Incidental Duties:
The above statements describe the general nature and level of work being performed in this job. They are not intended to be an exhaustive list of all duties, and indeed additional responsibilities may be assigned, as required, by management.

Job requirements

Qualifications:

Ability to work in a fast-paced environment with changing priorities.

Strong problem-solving skills and ability to follow detailed instructions.

Basic math skills (addition, subtraction, multiplication, division, fractions, decimals) and ability to compute rates, ratios, and percentages.

Ability to interpret graphs and apply common sense understanding to standardized situations.

Education and Experience:

High School diploma or equivalent required.

Minimum of two years of relevant experience in quality assurance required, preferably in the Medical Device or Pharmaceutical industry or technical field.

Skills and Abilities:

Experience with electronic systems (e.g., Oracle, SAP, Access, Excel).Understanding of product specifications, functionality, structure, assembly, and test methods.

Proficient in Microsoft Office Suite (Word, Excel, Outlook).Effective verbal and written communication skills in English.

Ability to handle and inspect small components.

Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Employees are required to sit at a desk for long periods of time Position requires occasional standing for periods of time Position requires occasional walking for short periods of time

The noise level in the environment is moderatePPE
- Safety glasses required worn by all personnel in production areas or as indicated undefined#LI-TP1

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Target Market Salary Range:

Actual compensation…