Quality Inspector I

Job Description :Quality Inspector I (Temporary)Location: Englewood, CO (100% Onsite)Company: Zimmer Biomet – Paragon 28 DivisionParagon 28, a Zimmer Biomet company specializing in innovative foot and ankle orthopedic medical devices, is seeking a detail-oriented Quality Inspector I to join our Quality Lab team. This role is responsible for inspecting raw materials, work-in-process, assemblies, and finished medical devices to ensure compliance with established quality standards and specifications. The successful candidate will support product release activities through accurate inspection, documentation, and quality assurance processes.Key ResponsibilitiesPerform receiving, in-process, and final inspections of materials, components, assemblies, and finished products.Conduct visual inspections in accordance with documented specifications and inspection procedures.Measure product features using precision measuring equipment and inspection tools.Complete inspection records and associated documentation to support product release.Identify, document, and segregate nonconforming materials in accordance with quality procedures.Monitor and verify calibration status of inspection equipment.Review, verify, scan, and file quality documentation as required.Assist with product identification, status tracking, and organization of inventory.Support product labeling and packaging activities when needed.Maintain compliance with company quality systems, SOPs, and regulatory requirements.Perform additional duties as assigned.Required QualificationsHigh School Diploma or equivalent.1–2 years of quality inspection experience in a manufacturing environment.Experience using dimensional measurement equipment such as:CalipersMicrometersGage PinsDial IndicatorsAbility to read and interpret engineering drawings and specifications.Basic understanding of GD&T (Geometric Dimensioning & Tolerancing) per ANSI Y14.5.Strong attention to detail and ability to inspect small, precision components.Good written and verbal communication skills.Basic proficiency with Microsoft Word and Excel.Ability to follow standard operating procedures and work instructions.Preferred QualificationsAssociate degree in a technical or related field.Experience with CMMs, Vision Systems, or other advanced inspection equipment.Knowledge of FDA 21 CFR Part 820, ISO 13485, or other regulated quality standards.Experience working with machined components and precision manufacturing processes.Medical device industry experience preferred.Key SkillsQuality InspectionIncoming, In-Process & Final InspectionPrecision MeasurementGD&T InterpretationNonconformance DocumentationCalibration VerificationMedical Device Quality SystemsAttention to DetailDocumentation & Record KeepingRegulatory ComplianceCompany Description Founded in 2015 and backed by two decades of hands-on experience, our strong insight on the enterprise ecosystem and its dynamics helps to offer a complete end-to-end solution. We automate recruitment processes with intelligent solutions to save time and money. Synkriom leads the industry with experience authentication of candidates. Company Description Founded in 2015 and backed by two decades of hands-on experience, our strong insight on the enterprise ecosystem and its dynamics helps to offer a complete end-to-end solution. We automate recruitment processes with intelligent solutions to save time and money. Synkriom leads the industry with experience authentication of candidates.