QC Inspector 2 **Date:** Jan 17, 2025 **Location:** Chelmsford, MA, US **Company:** Teleflex **Position Summary** With limited supervision performs quality inspections for IAB-C. Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in Principal Responsibilities. **Principal Responsibilities** • Compliance to all work instructions, Quality regulations, SOP’s, WI’s, GMP’s and GDP’s in the effort to manufacture high quality medical devices at all times. • Training: As required, will train employees to inspection requirements and techniques in manufacturing or other areas. • Retrieval of documentation or work instructions through Agile as necessary, to perform inspections. • Reviews orders and job packets, recording batch numbers and quantities, as required by inventory system. • Communication: shares instructions and knowledge with other inspectors or employees within the quality department. • Records results in a legible and accurate manner. • Reads, interprets and applies dimensional or other requirements defined in work instructions, process documents or graphics. • Provides support for special projects and assignments, including work in areas such as validations, nonconformance investigations and CAPAs. • Serves on and is actively involved in cross-functional teams. Interface, when needed, with various levels of manufacturing or engineering regarding quality issues. • Uses required tools and instruments (i.e. caliper, plug gauges, multimeter, microscope, and micrometer) to measure, assess or analyze quality attributes. • Inspect IAB and RH sub-assemblies and assemblies for cosmetic and physical flaws and/or perform electrical, mechanical and visual inspections of sub-assemblies and final assemblies. • Support in process and Final Inspection. • Adhere to and ensure the compliance of Teleflex’s Code of Ethics, all company policies, rules, procedures and housekeeping standards. **Education / Experience Requirements** • High School Diploma/GED **Specialized Skills / Other Requirements** • Minimum of six months of quality experience, preferably in medical device. • Experience with Quality Management Systems (ISO 13485 and Medical Device Regulations (21 CFR 820). • Must possess Quality job knowledge, including inspection, testing and record keeping. • Must be proficient in basic computer skills, Microsoft Office and SAP experience preferred. • Excellent Communication Skills • Must be extremely detail-oriented.