Sr.QA Technician - (Job Number: 0805072)

Sr.QA Technician - (Job Number: 0805072) DescriptionCordis Corporation, a member of Johnson && Johnson's Family of Companies is recruiting for a Sr. QA Technician, located in Warren, NJ. Ground breaking, life changing careers that reward the power of ideas and innovation. For more than 40 years, Cordis Corporation has pioneered less invasive treatments for vascular disease. Technological innovation and a deep understanding of the medical marketplace and the needs of patients have made Cordis the world's leading developer and manufacturer of breakthrough products for interventional medicine, minimally invasive computer-based imaging, and electrophysiology. Today, over 7,000 Cordis employees worldwide share a strong commitment to continue the Company's groundbreaking work in the fight against vascular disease.Cordis Corporation offers tremendous opportunities and world-class resources. Our decentralized structure provides the feel of a small-company environment with big-company impact. We are focused on developing leaders with a broad base of business and cultural skills, along with a strong commitment to the values expressed in Our Credo. By choosing Cordis Corporation, you are choosing to positively impact the lives of millions of people each year. The Sr. QA Technician under limited supervision, performs and documents moderately complex technical functions relating to test, quality control, layout, fabrication, modification and assembly of mechanical equipment and/or components. Performs electrical, mechanical, electromechanical, developmental or test technician duties in such areas as manufacturing, maintenance, quality, testing, engineering, where some judgment is required. Constructs, inspects, calibrates, adjusts, tests and maintains equipment, components, devices and systems. Summary reports, analysis of technical data, evaluation of quality control data and instrument troubleshooting are fully within the scope of this position. Utilizes a wide variety of developmental/manufacturing tests or diagnostic test equipment to check out, test, trouble shoot and maintain tools components, instruments, test apparatus and associated specific discipline equipment. May assist more senior technicians and engineers in specific discipline. Performs and documents moderately complex operational functional testing, troubleshooting and debugging of components, subassemblies, materials and manufacturing systems to isolate faults and determine remedy for malfunctions. Writes moderately complex technical reports and develops charts, graphs, and schematics to describe and illustrate systems/tests operating characteristics, malfunctions, deviations from design specifications, and functional limitations. Troubleshoots electrical, test, mechanical, facilities or hydraulic systems, components, and equipment. May provide guidance to lower level technicians. Performs moderately complex process/product tests and audits for conformity to quality and/or regulatory requirements. Performs selfinspections of own work. When applicable, follows standard operating procedures for all tasks. AA or equivalent; or trade/technical schooling; and 5-9 years of related experience and/or training; or equivalent combination of education and experience is required. Previous/current experience in the medical device industry is required. Previous Laboratory experience in an R&&D environment is preferred. Testing experience is also preferred. Experience with instrumentation is preferred. Ability to use sophisticated test and measurement equipment associated with specific discipline is preferred. Reads and understands technical documentation associated with specific discipline. Ability to use PC and associated software packages. Ability to read, write, communicate and understand English is required. Must be able to successfully complete company/department training courses in manufacturing techniques. Thorough understanding and application of federal regulatory requirements (21 CFR Part 11 Electronic Records; Electronic Signatures, 211cGMP for Finished Pharmaceuticals and 820 Medical Devices; Current Good Manufacturing Practice (cGMP). Apply Now