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Process Quality Technician - 2 openings

Company: Johnson & Johnson
Location: San Angelo
Posted on: September 10, 2019

Job Description:

Ethicon Inc. is recruiting for a Process Quality Technician.Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit the guidance of the Process Quality Leader or Manufacturing Manager, the Process Quality Technician provides technical support to identify the causes for non-conformances and process failures and to implement corrections thus assuring process performance and compliance against Ethicon's QSR, GMP, and ISO requirements for the manufacturing process. Under minimum supervision, established procedures and practices and clear-cut policies, exercises initiative and ingenuity to deal with varying circumstances, changing conditions, and proceeds when general instructions and established methods indicate action to be taken, referring unusual problems to supervisor.Work is generally diversified. Requires judgment in the application of broader aspects of established practices and procedures to problems and situations not falling clearly or concisely within the limitations of accepted standards or precedents. Work toward assigned objectives sometimes adapting or modifying methods and standards to meet variation in controlling conditions.You Will Under the guidance of the Process Quality Leader or Manufacturing Manager, performs non-conformance investigations including NCR origination, bounding, product control, failure investigation, correction, and documentation within the non-conformance system. Owns periodic review and SOP creations, Revisions for CME area. Leads small kaizens with cross functional teams to assure causes of non conformances are identified and understood and that sound corrective/preventive actions are implemented. Utilizes failure analysis tools (i.e. 5M analysis) to conduct robust investigations. Analyzes data and recommends actions for process, equipment, and system improvement. Provides recommendations for the enhancement of processes and systems. Utilizes document change control system to update procedures and write protocols. Implements corrections and process improvements. Provides training and education to the manufacturing team(s) as needed Acts in accordance with safety regulations and procedures. Supports internal and external audits and inspections. Provides leadership to other technicians and wage associates. Assists Facilitator on day-to-day activities. Accepts or initiates special projects. Plans and organizes assignments to ensure completion of projects in a timely fashion after receiving minimal instructions as to content and objective. Demonstrates excellent communication skills. Clear and concise oral and written communication skills are required to effectively communicate work requirements. Complies with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001).Qualifications Vocational, Certificate, Technical or Associates or Equivalent required A Bachelor's preferred 2 years of experience in the QSR/ISO regulated medical device operation preferred. Strong computer skills and use of software application(s). Experience with Word and Excel required. Experience with Minitab preferred. Basic statistical and analytical problem-solving skills required; experience with problem solving tools such as DMAIC, Fishbone Analysis, 5 Whys is preferred. Proficient in the preparation of technical reports and presentations. Strong communication and interpersonal skills. Requires good networking and influencing skills. Entails significant interaction with technical peers and manufacturing associates. Self-motivated and capable of completing job duties with limited supervision. Capable of serving as back up Facilitator when Facilitator is not available. The site is a 24/7 operation; weekends and holidays are included in the work schedule. This position will be scheduled to work off-shifts outside of the regular 8am-5pm M-F work schedule. Must be available to work night shifts.Physical Working Conditions Requirements Standing/Walking 3-4 hours at one time; total 9 hours per shift Bending/twisting/stooping 5-10 minutes at one time Sitting 1-2 hours per shift Pushing/pulling done occasionally Handling/fingering/keying/precision work done frequently Lifting/carrying up to 20lbs Occasionally Reaching over shoulder done occasionally Perform visual checks near and far. Hearing, speaking and reading required at all times. May work alone occasionally May require shift rotation. The noise level in the work environment is usually moderate. Associates is required to wear gowning as per established Quality Procedures.Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.Primary LocationUnited States-Texas-San Angelo-OrganizationEthicon Inc. (6045)Job FunctionProductionRequisition ID3536190830

Keywords: Johnson & Johnson, San Angelo , Process Quality Technician - 2 openings, Professions , San Angelo, Texas

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