About MedTech
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness.
About Surgery
Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that's reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world's most prevalent conditions such as obesity, cardiovascular disease and cancer.
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
We are searching for the best talent for SENIOR MANUFACTURING SYSTEMS ENGINEERING TECHNICIAN.
Purpose
The Manufacturing Systems Engineering Technician is a technical expert on MES (Manufacturing Execution System) software, CAMSTAR Manufacturing and Operational Intelligence Platform, capable of supplying support and troubleshooting skills to solve problems for the business units during and after an MES implementation and updates. Must be able to perform configuration changes on MES software per business needs.
You will be responsible for
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines, this position:
•Collaborates with the administration, problem solving and continuous improvement of MES.
•Establishes and instructs MES procedures for system users.
•Contributes to the development, tests, validations, and implementation of MES.
•Under the guidance of a supervisor and only when requested by his/her supervisor, aids the development, tests, validations, and implementation efforts of MES within other J&J (Johnson & Johnson) partners.
•Under the guidance of a supervisor, takes part and accelerates the completion of nonconformance activities.
•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 / Requirements
•Experience in a manufacturing environment and/or medical device industry preferred.
•A minimum of associate's degree in a Computer Science or related field.
•Strong proven experience in MES software administration (Camstar, ERP (Enterprise Resource Planning), AQR (Automated Quality Record)).
•Experience in Camstar configuration (WF, BOP (Bill of Process), E-procedure, Task list, UDCD, queries) preferably.
•Experience on troubleshooting Personal Computers (PCs) and the different device drivers, controllers, preferably.
Education
•Associate's degree in computer science or related field.
•Intermediate English Level is preferred.
Job Experience
•Approximate experience, or equivalent knowledge and skills, necessary to satisfactorily perform the position responsibilities.
•4 to 6 years' experience in manufacturing/design engineering.
Required Knowledge, Skills, Abilities, Certifications/Licenses and Affiliations
•Strong PC (Personal Computer) experience needed.
•Experience in CAMSTAR Software configuration.
•Position requires excellent communication skills plus the ability to function in a team-based manufacturing environment.
•Knowledge of information systems including but not limited to ERP, Quality Systems & Documentation Control Systems.
Desired/Preferred Qualifications
•Lean certification is preferred.
•Knowledge of equipment validation documents (IQ (Installation Qualification) or equivalent).
•Knowledge of GxP (Good x Practice) software validation (SDCL method).
Preferred Skills
Agile Manufacturing, Agility Jumps, Communication, Data Analysis, Equipment Maintenance, Good Manufacturing Practices (GMP), Issue Escalation, Manufacturing Equipment, OSHA Compliance, Plant Operations, Predictive Maintenance, Problem Management, Problem Solving, Project Management, Repair Management, Report Writing, Safety-Oriented
