Location: Salt Lake City,UT, USA
Quality Technician - Reagent Quality (C Shift)Location: Salt Lake City, UT, United States Position Type: Unfixed Term Job Function: QualityShare: share to e-mail Share on Facebookshare to facebook Tweetshare to twitter Share on LinkedInshare to linkedinApply Now >A world leader in the field of in vitro diagnostics for more than 60 years, bioMerieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 6,200 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics and one subsidiary in Montreal, Canada. Come and join a family-owned global company with a long-term vision, and a human-centered culture.Description A world leader in the field of in vitro diagnostics for over 55 years, bioMerieux provides diagnostic solutions which determine sources of disease and contamination to improve patient health and ensure consumer safety.In North America we have more than 5,000 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics. Come and join an amazing global company with a solid long-term vision and excellent human-centered culture as a Quality Technician!Job Summary The overall SLC Quality Assurance (QA) department provides Quality support across various departments, and is organized into distinct subunits, including Reagent Quality, Metrology, Calibration and Preventive Maintenance, Document Control, Quality Auditing, Instrument Quality, Servicing Quality, Incoming Material QC, etc.This is an entry-level position on the Reagents Manufacturing Quality Assurance (QA) team. This individual will primarily review quality records and inspect manufactured products but may also contribute to other quality functions. Timely and accurate work is expected. This position regularly interacts and collaborates with other departments within the company.ESSENTIAL JOB DUTIES AND RESPONSIBILITIES * Perform all work in compliance with company policy and within the guidelines of its Quality System. * Responsible for reviewing, assessing and monitoring process and product to ensure compliance to requirements. * May contribute to other Quality Assurance subunits that are outside of their primary Quality Assurance subunit, as assigned. * Inspect product (including labels) to specifications and established procedures. Determine product acceptance status after inspection. * Identify and escalate non-conformances observed during inspection. Work with production teams to resolve non-conformances where possible. * Ensure good documentation practices during quality document and quality record review. Report inconsistent or incorrect records to appropriate systems. Work with production teams to resolve erroneous records. * Physically release work in process for finished goods processing. * File and archive quality records according to established processes. * Prioritize product release to meet department goals. QUALIFICATIONSTraining and Education: * High school diploma or equivalent is required. * Knowledge of good manufacturing practices, ISO 9001, ISO 13485, and/or 21 CFR 820 is preferred. Experience: * Minimum 1-year previous on-the-job experience requiring professional communication and interactions utilizing skills outlined below. * Experience in Quality Assurance or Quality Control, laboratory or life science manufacturing setting that has a formal quality system is preferred. Knowledge, Skills, and Abilities: * Effective written and verbal communication skills * Proficiency in MS Office tools, including Outlook, Word, and Excel * G eneral computer operation * Attention to detail is fundamental to this position * Ability to... For full info follow application link.#AdvancedManufacturing #Manufacturing