Quality Assurance Inspector II

Engineered Medical Systems (EMS) is a full-service medical device manufacturer dedicated to precision, innovation, and quality. From our state-of-the-art facilities, we specialize in precision machining, complex assembly, and advanced manufacturing technologies—all tailored to meet the rigorous standards of the medical industry.

Beyond our technical capabilities, EMS fosters a collaborative and quality-driven culture where craftsmanship, continuous improvement, and team empowerment are at the core of everything we do. Our people are our greatest asset, and we take pride in cultivating a workplace that values integrity, accountability, and shared success.

Our services span prototype development, design verification and validation, full-scale production, and custom solutions. With a team-focused approach, we enhance design functionality, manufacturability, and product reliability—bringing premium medical devices to market with confidence and care.

Learn More About Us Here!

The Quality Assurance Inspector II will be inspecting product to assure that it meets or exceeds the requirements set forth by customer specifications and quality acceptance criteria.

Responsibilities

• Perform first article, in-process, and final product inspection using drawings, specifications, and / or related instructions.
• Read manufacturing prints and determine relevant features for verification of accuracy.
• Understand and complete Document Review Checklist (DRC) and Quality Inspection Report (QIR) accurately.
• Capture results data and store electronically in correct file folders.
• Correctly utilize / interpret generalized inspection equipment, to include micrometers, calipers, comparators, and related gages and equipment. May be involved in inspecting parts using advanced inspection equipment.
• Check out and return gages for each inspection.
• Assist with customer concerns and inquiries as they relate to product quality at EMS.
• Assist and / or instruct manufacturing personnel with checking product correctly as it relates to the customer inspection criteria.
• Maintain strict focus on accuracy, neatness, and thoroughness of product inspection and documentation of results.
• Identify non-conforming product and may complete or escalate to management non-conforming paperwork and product per requirements.
• Record production through Job Boss system.
• Performs other job duties as assigned.
• Support of the EMS Quality Policy and Quality Objectives.

This team member supports various activities that contribute to the overall EMS objective of compliance to FDA regulations & ISO 13485 requirements. Ongoing collaboration with additional EMS roles is required.

Requirements

Restrictions

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I certify that all the information on this application, my resume, or any supporting documents I may present during any interview is and will be true, complete and accurate, to the best of my knowledge. I understand that any falsification, misrepresentation, or omission of any information may result in disqualification from further consideration for employment or, if employed, disciplinary action, up to and including immediate dismissal, regardless of when such information is discovered.

The Company considers this Application for Employment to be a part of the personnel record.

THIS COMPANY IS AN AT-WILL EMPLOYER WHERE ALLOWED BY APPLICABLE STATE LAW. THIS MEANS THAT REGARDLESS OF ANY PROVISION IN THIS APPLICATION, IF HIRED, THE COMPANY OR I MAY TERMINATE THE EMPLOYMENT RELATIONSHIP AT ANY TIME, FOR ANY REASON, WITH OR WITHOUT CAUSE OR NOTICE. NOTHING IN THIS APPLICATION OR IN ANY DOCUMENT OR STATEMENT, WRITTEN OR ORAL, SHALL LIMIT THE RIGHT TO TERMINATE EMPLOYMENT AT-WILL. I UNDERSTAND THAT NO COMPANY EMPLOYEE OR REPRESENTATIVE HAS THE AUTHORITY TO ENTER INTO A CONTRACT REGARDING DURATION OF TERMS AND CONDITIONS OF EMPLOYMENT OTHER THAN THE PRESIDENT / CEO OF THE COMPANY AND THEN ONLY BY MEANS OF A WRITTEN CONTRACT SIGNED BY THE PRESIDENT / CEO.

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If hired by the Company, I understand that I will be required to provide genuine documentation establishing my identity and eligibility to be legally employed in the United States by this Company as required by the Immigration Reform and Control Act of 1986. I also understand this Company employs only individuals who are legally eligible to work in the United States.

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