Aptus Endosystems offers a dynamic, fast-paced working environment and the chance to be a part of an experienced, high-performance team of professionals. We offer competitive compensation packages and professional growth opportunities.
Aptus Endosystems is an equal opportunity employer.
If you are interested in joining our team, have the drive and experience in the development and advancement of new medical technologies, then submit your resume to
Quality Inspector
General Summary:
Perform inspections, checks, tests, and sampling procedures of components, assemblies and finished medical devices.
Essential Functions:
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Perform inspections of components, sub-assemblies or finished company products according to documented criteria using standard physical, mechanical, and/or electrical measurements.
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Identify nonconforming subassemblies or finished products as required, and document according to established policies and procedures.
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Conduct and document process and system audits using written procedures as audit standards.
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Accurately document the results of inspections and testing.
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Maintain all controlled document files and test records in a timely and accurate manner.
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Monitor critical equipment and instrumentation to ensure proper operation and calibration.
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Participate in the construction and/or revision of Quality System documents for the inspection function.
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Assist in writing and updating inspection procedures, protocols, and checklists.
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Evaluate problems and make initial recommendations for possible corrective action to supervisor.
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Perform data entry into MRP system.
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Work with production management and QA to provide feedback to assemblers regarding accuracy of assembly procedures.
Skill Requirements:
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Good math and verbal/written communications skills. Computer literacy is required.
Education/Training/Experience Requirements:
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High School graduate equivalent required. AA in a technical field preferred. 2 to 4 years minimum experience in manufacturing required, preferably in medical devices.
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Basic understanding of domestic and international statutory regulations (cGMP/QSR, MDD) and voluntary standards (ISO 9000/13485).
Preferred Experience:
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Experience with MRP System is a plus.