The Quality Control Inspector II is responsible for performing routine inspections of components, subassemblies, and finished products to ensure compliance with approved drawings, specifications, inspection plans, and regulatory requirements. This role supports product quality, safety, and effectiveness while maintaining compliance with current Good Manufacturing Practices (cGMP), FDA Quality System Regulations (21 CFR 820), and other applicable quality standards. Working knowledge of c

GMP, FDA

quality system regulations, and quality inspection practices in a regulated environment. Ability to interpret drawings, specifications, and inspection methods. Working knowledge of 21 CFR 820, ISO 13485, EU MDR, MDSAP, and other global standards Experience and ability in reading and interpreting engineering drawings. Proficiency using inspection tools and measuring equipment. Experience using vision systems and other automated inspection systems. Strong attention to detail and accuracy. Strong organizational, interpersonal, verbal, and written communication skills (clear, concise, effective with a variety of stakeholders). Must be proficient in the use of Microsoft Excel, Microsoft Word, Outlook, and PowerPoint. Strong organizational, troubleshooting, and problem-solving skills. Perform routine and detailed inspections of incoming materials, in-process goods, and finished products. Conduct visual, dimensional, mechanical, and functional inspection using approved methods, tools, and equipment. Ensure components, subassemblies, and finished products comply with approved company drawings and specifications. Document inspection results to ensure full traceability. Identify, document, and report defects or nonconformances (NCMRs) Provide guidance for less experienced team members Support Site Quality Management in determining disposition of product (accept, reject, rework, return to vendor) in accordance with approved company procedures. Collaborate cross-functionally to assist with investigations and resolve potential quality issues. Support corrective and preventive action (CAPA) activities. Participate in internal and external audits and inspections as required. Participate in other projects as required by Quality Management. Perform other duties as assigned.