About this role
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual.
At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Supply Chain Manufacturing Job Sub Function: Manufacturing Process Improvement Job Category: Business Enablement/Support All Job Posting Locations: Grecia, Costa Rica Job Description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation enables us to build a world where complex diseases are prevented, treated, and cured; where treatments are smarter and less invasive; and where solutions are personalized.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions and deliver the breakthroughs of tomorrow to profoundly impact human health. Learn more at https://www.jnj.com/ . About MedTech Driven by innovation at the intersection of biology and technology, we are developing the next generation of smarter, less invasive, and more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at Johnson & Johnson MedTech . About Cardiovascular Driven by innovation at the intersection of biology and technology, we are developing the next generation of smarter, less invasive, and more personalized treatments.
Are you passionate about advancing and expanding the possibilities of cardiovascular care? Ready to join a team that is reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke care.
You will become part of a proud legacy of continuously raising the standard of care for patients living with stroke, heart failure, and atrial fibrillation (AFib). We are looking for the best talent for the position of Manufacturing Process Failure Analyst Purpose: Independently, or under limited or null supervision, works on complex by nature assignments, which require considerable criteria, judgment and initiative in order to solve problems and issue recommendations. The manufacturing process improvement technician is responsible for analyzing product failure tendencies, performing and keeping records of failure analysis and propose solutions / impart feedback to improve the manufacturing process within production lines.
They are responsible for ensuring that all activities assigned to them in designated manufacturing lines is performed, keeping the expected levels of the Department in the GMPs (Good Manufacturing Practices). Compliance with Good Manufacturing Practices (GMPs) making observations and communicating them to their supervisor for their correction. This position supports the Electrophysiology platform within J&J MedTech in manufacturing of electrophysiology cardiovascular products.
Duties & responsibilities In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: Provides solutions to the problems in manufacturing of current and new models. Performs basic operational diagnostics test. Solves problems and disconnects components, subassemblies and manufacturing systems, processes and equipment with the purpose of isolating failures, determining the solution and performing the necessary training.
Analyses the non-conformant product in the production line determines the root cause and proposes corrective actions working as a team with the manufacturing supervisor and with the engineering and quality departments. Starts, adjusts and operates basic laboratory and manufacturing equipment. Performs simple tests to the processes/products, as well as audits in compliance with quality and/or other regulatory requirements.
Conducts tests and basic evaluations, experimental tests and design proposal research under operational conditions. Records the procedures and results of the tests, as well as the numeric and graphical data for its revision by Operations. Can provide recommendations and technical support for new projects, process improvements and quality investigations.
Can support the diagnostic and analysis for product customer complaints; perform the awareness session for the operators and determines the root cause and proposes correction and corrective actions working as a team with the manufacturing supervisor, and with the engineering, quality and failure analysis laboratory departments. Can support the solutions to problems referring to the product in question, evaluating systems, components and electrical or testing equipment. Can support the solution to problems referring to the product Customer Complaints, evaluating systems, components and electrical or testing equipment.
Provides support to operators, group leaders and trainers, in areas related to the discipline. Performs inspections to their own work. Follows standardized procedures while performing their tasks, when applicable.
Follows the Convenient Information Retention Administration Policies of J&J and of the Campus, record retention program, training and education, Document Retention Notices, Record cleanup, inactive records and Information Management, Vital Records if applicable. Other responsibilities can be assigned and not all the responsibilities listed here must be assigned. Has completed the environment and safety training, appropriate for his/her discipline Responsible for communicating business-related issues or opportunities to next management level Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
For those who supervise or manage a staff, responsible for ensuring that 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, if applicable 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 / R equirements: Experience and education Technical Certificate Generally, Requires 2-4 Years Work Experience Preferred ability to communicate effectively in English and Spanish across functions and both internally/externally Required knowledge, skills, abilities, certifications/licenses and affiliations Ability for the resolution of failures, in aspects or areas of manufacturing. Ability to integrate into work groups. Knowledge of the product manufactured by the Company.
Ability to use measuring and testing equipment associated with specific discipline. Basic ability to read and understand technical documentation associated with specific discipline. Capacity to successfully complete the departmental/corporate courses of training in manufacturing techniques.
Ability to learn about regulatory requirements (GMP and GDP). Ability to use computers and related software. Ability to learn and adhere to specific procedures according to the department training plan Able to work in a Clean Room environment requiring gowning.
Must have strong communication and interpersonal skills and be able to support cross functional teams including Quality, Operations & Engineering. Responsibility for others & internal interactions This position reports to the Eng Workstream Sr. Manager Works with other departments such as Operations, Engineering, Quality to ensure that a variety of business transactions are completed Location & travel requirements Location of this position is J&J MedTech, Alajuela, Costa Rica on-site.
Travel might be required to other J&J locations worldwide #RPOCRA #LI-Onsite Required Skills: Preferred Skills: Accountability, Administrative Support, Agile Manufacturing, Chemistry, Manufacturing, and Control (CMC), Communication, Data Gathering and Analysis, Detail-Oriented, Document Management, Goal Attainment, Good Manufacturing Practices (GMP), Issue Escalation, Plant Operations, Process Control, Process Optimization, Process Oriented, Quality Management Systems (QMS), Quality Standards, Quality Systems Documentation, Time Management