QC Inspector 3 - 1st Shift

Position Summary

With limited supervision performs quality inspections for IAB-C.  Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in Principal Responsibilities.

Principal Responsibilities

•    Compliance to all work instructions, Quality regulations, SOP’s, WI’s, GMP’s and GDP’s in the effort to manufacture high quality medical devices at all times.
•    Training: As required, will train employees to inspection requirements and techniques in manufacturing or other areas.
•    Retrieval of documentation or work instructions through Agile as necessary, to perform inspections.
•    Reviews orders and job packets, recording batch numbers and quantities, as required by inventory system.
•    Communication: shares instructions and knowledge with other inspectors or employees within the quality department.
•    Records results in a legible and accurate manner.
•    Reads, interprets and applies dimensional or other requirements defined in work instructions, process documents or graphics.
•    Provides support for special projects and assignments, including work in areas such as validations, nonconformance investigations and CAPAs.
•    Serves on and is actively involved in cross-functional teams.  Interface, when needed, with various levels of manufacturing or engineering regarding quality issues.
•    Uses required tools and instruments (i.e. caliper, plug gauges, multimeter, microscope, and micrometer) to measure, assess or analyze quality attributes.
•    Inspect IAB and RH sub-assemblies and assemblies for cosmetic and physical flaws and/or perform electrical, mechanical and visual inspections of sub-assemblies and final assemblies.
•    Support in process and Final Inspection.
•    Adhere to and ensure the compliance of Teleflex’s Code of Ethics, all company policies, rules, procedures and housekeeping standards.
 

Education / Experience Requirements

•    High School Diploma/GED required.

Specialized Skills / Other Requirements

•    Minimum of six months of quality experience, preferably in medical devices.
•    Experience with Quality Management Systems (ISO 13485 and Medical Device Regulations (21 CFR 820).
•    Must possess Quality job knowledge, including inspection, testing and record keeping.
•    Must be proficient in basic computer skills, Microsoft Office and SAP experience preferred.
•    Excellent Communication Skills.
•    Must be extremely detail-oriented.

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