TECHNICIAN II - Biosense Webster-9684140429
Description
Biosense Webster, Inc (BWI), a member of The Johnson & Johnson Family of Companies, is recruiting for a Technician II in our Irwindale, CA location.
Hi-Tech meets Medical Devices at Biosense Webster! If you want to work with brilliant people in a fast paced environment, help make a huge difference in patient’s lives and want to be responsible for providing the most innovative technology in the field of cardiac electrophysiology, then Biosense Webster is the place for you! Our vision and mission are clear – be #1 in rhythm solutions globally and cure AF (Atrial Fibrillation), the most common heart arrhythmia. Our products are used by prominent physicians around the world and help improve thousands of patient’s lives. Simply put, we are a highly innovative entrepreneurial company with a truly global and diverse culture, backed with the support structure of the Johnson & Johnson Corporation – quite a winning combination! Our commitment to quality and our Credo have helped us achieve significant milestones as a company.
Biosense Webster is the world leader in the worldwide electrophysiology market and our company is in the enviable position of being one of the fastest growing businesses within Johnson & Johnson. We have achieved double digit growth consistently over the last decade and aren’t stopping as we look towards the future. Our product portfolio remains strong and further proves we are an innovative leader in cardiac electrophysiology. In order to continue this great growth trajectory, we need to bring on board top talent like you to help fuel our future! Our growth has also enabled a relentless focus on talent development by providing many new opportunities for our employees to expand their knowledge and grow their careers. Our commitment to developing our leaders is unwavering. Our investment in people, technology, and innovation make us one of the best places to work within one of the most admirable corporations in the world.
Under close supervision, performs and documents somewhat simple technical functions relating to test, layout, quality control, fabrication, modification and assembly of mechanical equipment and/or components. Performs electrical, mechanical, electromechanical, developmental or optical technician duties in such areas as manufacturing, maintenance, quality, testing, engineering, development, where some judgment is required. Constructs, inspects, calibrates, adjusts, tests and maintains equipment, components, devices and systems.
Under close 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 also 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; Maintain and repair (when necessary) manufacturing equipment; Support less experienced manufacturing technicians; Perform evaluations for supervisor/engineer with minimal instruction; Able to perform relatively complex inspections utilizing test equipment; Audit workstation practices to ensure compliance; Implement manufacturing efficiency and quality improvements; Responsible for communicating business related issues or opportunities to next management level; Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition; Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures; Performs other duties assigned as needed.
Qualifications
This role requires a minimum of three years or more experience in the manufacture of medical devices and/or solid state materials, and electronics. A minimum High School Diploma or GED is required, Associate Degree or higher is a plus. Proficiency in Microsoft Office is required, as is experience with mechanical and electrical assembly. GMP and experience with AutoCAD or SolidWorks is preferred. Six sigma and process excellence tools/methodologies experience is an asset. Must have good to excellent organizational skills, must be thorough and detail oriented, must be able to successfully complete company/department training courses in manufacturing techniques with the ability to learn regulatory (GMP) requirements. Must be able to work with a minimum of supervision, and must have good to excellent reading, writing and communication skills in the English language. Weekend and overtime work may be required. The employee is required to wear special garments when working in a clean room environment, and is also required to work 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, and noise levels may be loud. Qualified candidates should have the ability to commute daily to the Irwindale, CA facility.
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Primary Location:North America-United States-California-Irwindale
Organization: Biosense Webster Inc. (6010)
Job Function: Production
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