The QC Engineering Technician conducts activities within the Quality Control functions testing and release of finished product and any applicable in-Process audits (ensuring that manufacturing operations remain in control). This job serves as the lab technician in the QC group and entails ensuring availability of materials for QC testing, organization of lab processes and ensuring equipment is maintained / calibrated as appropriate, and departmental documentation is current and accurate. Responsible for ensuring deviations are properly documented, nonconforming material is segregated and secured, and the supporting of any projects assigned. Performs all duties using safety conscious practices. Individual must inspect/test/audit materials & processes in a timely fashion while, at the same time, ensuring conformance to all requirements. Job responsibilities: + Perform all work in compliance with company quality procedures and standards. + Performs QC testing on finished products, prepares reports and submits for review to Quality Manager for release. + Performs a wide variety of inspection, audit and release activities. + Inherent in the process of inspection is the interpretation of requirements, and the need to use careful judgment to determine compliance. It is critical for individuals in this role to use sound judgment, and demonstrate consistent decision-making. + Performing the QC testing routinely results in the need to investigate nonconformances, and either independently address them, or interface with technicians and/or engineers to diagnose and remedy the problem. + Understands operational priorities and organizes QC activities accordingly to meet the needs. + May be responsible for the timely setup and inspection of components, raw materials, in-process, and release of finished product in accordance with specifications. Interprets blueprint requirements and confirms conformance to specifications. Leads in the standardization and advancement of inspection methods. Train new and existing QC Technicians. + Transport conforming parts to inventory, including all computer transactions and written record completion. For materials found to be nonconforming, generates “nonconforming material reports”, requiring a technically accurate description of the anomalies. + Responsible for ensuring nonconforming, Line Throw Off, and Purged material is segregated and secured including the disposition of non-conforming materials meet all necessary site and regulatory requirements. + Perform Quality Control in-process inspections & audits necessary to support Instrument Manufacturing. Assesses subassemblies, finished devices, and the assembly & test processes for conformance to documented requirements. + Responsible for ensuring that QC Inspection Methods are current and accurate. + Maintains thorough understanding of all specifications, requirements, and procedures and provides input regarding the continuous improvement of each. Minimum Requirements: + Technical degree in Biology or related field and 0-2 years of work experience in a Quality Control setting preferred. 2 years experience in a Quality Control Department will be accepted in lieu of the degree Skills and Knowledge: + Hands on experience with PCR, Aseptic technique, Microbiological Media and reagent preparation, Propagation and enumeration of microbial cultures, DNA and RNA isolation, purification and quantification is preferred + Experience working in BSL2 work environment preferred + Ability to effectively communicate written and verbally. + Requires strong interpersonal skills to interacts with all levels of the organization. Also requires a strong analytical approach to decision making and problem solving. + Competence in the use of Quality Dimensional Tools and Techniques and advanced knowledge of quality systems (SAP/LIMS/Trackwise) is a plus. + Requires strong computer skills including Microsoft Office Package (Excel, Word, etc.). + Familiarity/knowledge of the interpretation and application of relevant Domestic and International Regulations and Industry Standards (ISO, QSR, UL, CSA, VDE, etc.) preferred.