Principal Technician

DescriptionBiosense Webster, Inc., is currently recruiting for a Principal Technician to be located in Irwindale, CA. Biosense Webster, Inc., is recognized worldwide as an industry leader in endocardial diagnostics and therapy. Guided by the needs of electrophysiologists and cardiologists, the company has pioneered innovative technological advancements ranging from the first deflectable tip catheter to today's most sophisticated three-dimensional cardiac mapping and navigation systems. Biosense Webster, Inc., combines leading-edge technology with a tradition of quality and responsiveness while partnering with the physician to optimize patient outcomes. Under limited supervision, performs and documents complex technical functions relating to test, quality control, lay??'out, 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. ESSENTIAL DUTIES AND RESPONSIBILITIES Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, the duties of this position may include:Monitor and document manufacturing processes; Work with engineers to develop new products and processes; Build and test prototypes; Test and validate new products and/or equipment; Offers suggestions for improvement in operating time, yields, ergonomics, handling, etc; Write or update work instructions, part specifications, validation protocols, test reports, service reports, routine reports and correspondence, develop, proof read and update technical documents (ECOs, cPDM); Identify production problems, evaluate, and recommend solutions and methods of improvements; Actively support Operation's programs of continuous improvement; Train associates to manufacturing operations, to certified operations, documentation, and regulatory requirements. Suggestions revision/changes to manufacturing documents as appropriate. This position will also: Maintain and repair (when necessary) manufacturing equipment; Support less experienced manufacturing technicians; If required, supervise line operators including responsibility for all daily tasks. Additionally this role will need to perform evaluations for supervisor/engineer with minimal instruction, and be able to perform complex inspections utilizing test equipment, audit workstation practices to ensure compliance, implement manufacturing efficiency and quality improvements. QualificationsA minimum seven years or more experience in the manufacture of medical devices and/or solid state materials, and electronics, and an Associates or equivalent; or trade/technical schooling; or equivalent combination of education and experience is required.Must be Microsoft Office proficient, have experience with mechanical and electrical assembly, a thorough understanding of regulatory requirements (GMP) recomended. Experience with AutoCAD or SolidWorks is required, six sigma and process excellence tools/methodologies experience highly desired. This position will also require excellent organizational skills. Must be thorough and detail oriented. Must be able to successfully complete company/department training courses in manufacturing techniques.Weekend and overtime work may be required, the employee is required to wear special garments when working in a clean room environment, this role requires working with a variety of manufacturing equipment, While performing the duties of this job, the employee may work near moving parts and may be exposed to fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock. The noise level may be loud. This position is based in Irwindale, CA.