Quality Inspector II

Nissha Medical Technologies•Colorado Springs, CO

22d•$18 - $22•Onsite

About The Position

Nissha Medical Technologies is looking for a Quality Inspector II to join our Quality Team in Colorado Springs! The Quality Inspector II is responsible for verifying incoming raw materials, in-process, and final product to ensure that materials that do not conform to specification are prevented from being used or delivered. Maintains appropriate records to complete the evidence of conformance and performs the following essential functions and basic duties: ESSENTIAL DUTIES AND RESPONSIBILITIES (other duties may be assigned): General: Follow Employee guidelines and Quality System Regulations as defined by Nissha Medical Technologies practices, policies and Standard Operating Procedures to ensure that customer requirements and industry standards and or regulations are met. Demonstrates knowledge and acts in accordance of NMT's Employee Guidelines and applicable quality standards as outlined in NMT's Quality Manual. Abides by all safety and security rules set forth by the company and regulatory agencies Regular attendance is required Inspection: Verify that materials, parts, and assemblies procured from the following sources meet dimensional and visual characteristics as required by Standard Operating Procedures, Manufacturing Assembly Instructions (MAI), work instructions, Drawings, Specifications, and IQIR's: Incoming product and material Internal Set-up Verifications (SUV) Internal sub-assembly production for inclusion in finished product Collect, sort, summarize, file, and maintain inspection and test data on materials, processes, parts, assemblies, and finished products. Maintain a record keeping system to document the inspection and test process on materials. Collaborate with Engineering or other team members for correcting and/or disposition of nonconforming products. Support Quality Technicians with GR&R, first article inspections, and metrology requests as necessary. Additional Tasks: Responsible for performing and documenting in-process audits in production areas as assigned. Responsible for properly maintaining laboratory equipment and environment in Quality Lab. Responsible to train, or assist in training, of new employees on practices and procedures.

Requirements

Minimum 3 years of related experience, Medical Device preferred.
High School Diploma or General Education Degree (GED).
Must be highly organized, detail oriented and work effectively as both a team member and independent contributor.
Demonstrated proficiency in MD Suite, particularly Microsoft (MS) Word and Excel.
Ability to work independently with limited instruction.
Ability to read and interpret documents such as safety rules, operating and Maintenance instructions and procedure manuals.
Ability to write routine reports and correspondence.
Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form.
Ability to deal with problems involving several concrete variables in standardized situations.
Familiarity with standard inspection tools to include: calipers, micrometers, optical comparator, scales and pin gauges.
Frequently remain in a stationary position for long periods of time.
Regularly use hands and fingers to make small movements and handle small parts/tools.
Frequently reach with hands and arms.
Perform repetitive tasks using wrists, hands and fingers.
Occasionally move between buildings and offices (campus environment).
Constantly and successfully communicate with employees, managers, and members of the public, in person and on the phone, regarding sensitive matters.

Nice To Haves

COI certification preferred.
Vision System and CMM operation experience preferred.

Responsibilities

Verify incoming raw materials, in-process, and final product to ensure that materials that do not conform to specification are prevented from being used or delivered.
Maintain appropriate records to complete the evidence of conformance
Follow Employee guidelines and Quality System Regulations
Verify that materials, parts, and assemblies procured meet dimensional and visual characteristics
Collect, sort, summarize, file, and maintain inspection and test data on materials, processes, parts, assemblies, and finished products.
Maintain a record keeping system to document the inspection and test process on materials.
Collaborate with Engineering or other team members for correcting and/or disposition of nonconforming products.
Support Quality Technicians with GR&R, first article inspections, and metrology requests as necessary.
Responsible for performing and documenting in-process audits in production areas as assigned.
Responsible for properly maintaining laboratory equipment and environment in Quality Lab.
Responsible to train, or assist in training, of new employees on practices and procedures.