Manufacturing Systems Engineering Technician Iv - Ciudad Juarez, México - Johnson & Johnson

Johnson & Johnson

Empresa verificada

Ciudad Juarez, México

hace 2 semanas

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.

Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.

Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.

At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.

In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.

We are in this for life.
We are changing the trajectory of human health,
YOU CAN TOO.
We are searching for the best talent for
MANUFACTURING SYSTEMS ENGINEERING TECHNICIAN IV to be in
CIUDAD JUAREZ, CHIHUAHUA.

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:

Under limited supervision and 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 to his/her supervisor, she/he will aid the development, tests, validations, and implementation efforts of MES within other J&J (Johnson & Johnson) partners.
Under the guidance of a supervisor, she/he will take part and accelerate the completion of nonconformance activities.
Responsible for communicating business related issues or opportunities to next management level.
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:

EDUCATION AND EXPERIENCE:

Experience in a manufacturing environment and/ or medical device industry preferred.
A minimum of Associates 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), Eprocedure, Task list, UDCD, queries) preferably.
Experience on troubleshooting Personal Computers (PCs) and the different devices drivers, controllers) preferably.
Proficient English Level is preferred.

ADDITIONAL REQUIREMENTS:

Strong PC (Personal Computer (PC)) experience needed.
Experience in CAMSTAR Software configuration.
Position requires excellent communication skills plus the ability to function in a teambased 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).
Medical device or pharmaceutical industry experience