Inspector 2

Responsibilities:

Performs incoming, in process, and final inspections.

Performs visual, dimensional and functional inspections i.e. on a wide variety of products in accordance with internal procedures and Product Specifications.

Reports non-conformances to Supervisor and discusses corrective action.

In addition, follows-up to see if corrective action was effective.

Determines whether product is acceptable or rejected, initiates rejection notices, and maintains accurate written records of the inspections performed, including the results.

Recognizes conditions outside their specific areas of inspection which require action and refers the items to the supervisor.

Monitors compliance to G.M.P. and G.D.P. in employee working areas and reports infractions to Q.C.

Supervisor for corrective action. Employee evaluates both the product and process, making decisions on subjective visual inspections.

Responsibilities have an impact on product quality, productivity, and product costs as affected by internal and external costs of rework, scrap and product warranty.

High school diploma or GED.

One to two (1-2) years related Quality Control experience or equivalency.

Demonstrated human relation and communications skills.

Knowledge of inspection/sampling techniques and familiarity with ANSI/ASQZ1.4, AQL.

Knowledge of mechanical and physical inspection techniques using (calipers, micrometers, blueprint/artwork reading, etc.).

Must be able to read and comprehend English.

Duties require basic knowledge of math.

At least Six (6) months related work experience in a ISO 13485 / FDA medical device manufacturing environment preferred.

Ability to withstand repetitive motion and to lift up to 50 lbs.

Solid understanding of computers.