| A strong Scientific and technological pioneering spirit drives bioMérieux development since its creation in 1963. We design innovative in vitro diagnostic solutions for our customers that initiate new forms of scientific partnerships to be at the forefront of the most advanced technologies. Our presence in more than 150 countries with 9,400 employees worldwide secures bioMérieux commitment to public health. bioMérieux products are used to diagnose infectious diseases, they provide high medical value results for cancer screening and monitoring, cardiovascular emergencies and contamination to improve patient health and ensure consumer safety. Products also include industrial microbiological controls to detect microorganisms in food, pharmaceutical and cosmetic products. We are committed to creating an optimal work environment that fosters teamwork, emphasizes training and offers international career development opportunities. MAIN ACCOUNTABILITIES · Perform Incoming inspection: Set up and inspect parts and materials, interpreting blueprint requirements, choosing the proper inspection equipment and techniques, and confirming conformance to specifications. This responsibility includes determination of the proper sample size, and stratifying the lot of materials to obtain a representative sample to inspect. · Control Nonconforming Material: Transport conforming parts to inventory, including all necessary computer transactions and written record completion. For materials found to be nonconforming, this responsibility includes the generation of “nonconforming material reports”, requiring a technically accurate description of the anomalies. · Conduct Manufacturing Audits: Perform Quality Control in-process inspections & audits necessary to support Instrument Manufacturing. This responsibility includes assessment of subassemblies, finished devices, and the assembly & test processes for conformance to documented requirements. · Execute Product Release: Perform final inspections of completed medical devices and accessories, including the detailed review of the Device History Record package to confirm the completeness and accuracy of records prior to formally releasing the instrument for distribution. · Perform First Article Inspections: on complex mechanical & electrical parts. This responsibility includes interpreting blueprint requirements, choosing the proper inspection equipment and techniques, and confirming conformance to specifications. · Temporary modification to provide reasonable accommodations do not waive any essential functions of the job requirements. · bioMérieux Behaviors, including: Reasonable, reliable attendance and punctuality is an essential job function required for this position. Qualifications KNOWLEDGE AND EXPERIENCE REQUIRED FOR THE JOB:
bioMérieux is an Equal Opportunity, Affirmative Action Employer. M/F/Vet/Disability/Sexual Orientation/Gender Identity. Primary Location : AMER-AMER-US-MO-St. Louis, MO Schedule : Full-time Job Posting : Jun 14, 2017, 10:58:46 AM Shift : Day Job Employee Status : Regular Travel : No |
