Mes Validations and Sdlc Specialist - Ciudad Juarez, México - Johnson & Johnson
Descripción
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities, and forward progress.That's why for more than 135 years, we have aimed to keep people well at every age and every stage of life.
Today, as the world's largest and most broadly based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, create healthier communities, and put a healthy mind, body, and environment within reach of everyone, everywhere.
Every day, our more than 140,000 employees across the world are blending heart, science, and ingenuity to profoundly change the trajectory of health for humanity.
Diversity, Equity & 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.We are searching for the best talent for MES VALIDATIONS AND SDLC SPECIALIST (TEMPORARY 8 MONTHS) to be in Ciudad Juarez, Mx.
Job Summary:
You will be responsible for:
Under limited supervision and in accordance with federal, state, and local laws/regulations and Johnson & Johnson Corporate Procedures and Guidelines, this position:
- Performs advanced tasks consisting primarily of responsibilities to support industrial engineers and
- Build products and subassemblies for testing, prototyping, and product or process improvements.
- Performs periodic preventive maintenance and calibration of the MES equipment. He works
- Identifies problem requirements, breaks down problems into manageable, discrete components, and
- Creates and maintains engineering documentation, such as document change orders, validations,
procedures.
- Performs basic process validations and process improvements, solves problems, and makes
- Consult with engineering and other personnel on manufacturing capabilities, production schedules, and
- Assists in the engineering of complex tools to aid in the manufacture of the device and assists in
- Is responsible for communicating businessrelated matters or opportunities to the next managerial level
- For those who supervise or manage personnel, they are responsible for ensuring that subordinates follow
necessary resources to do so are available and in good condition, if applicable.
- Is responsible for ensuring personal and Company compliance with all Federal, State and Local company regulations, policies, and procedures
- Performs other assigned tasks as needed.
Qualifications:
Qualifications and requirements:
- Bilingual: English/Spanish
- Bachelor's degree in a related field.
- Usually, 6 to 8 years of work experience are required
- Knowledge in Lean tools, 6 Sigma
- Extensive knowledge of software validation methodologies, SDLC, CSV, GxP.
- Extensive knowledge of the capabilities and limitations of existing systems.
- Constant and continuous learning of the relevant technologies necessary to carry out their work.
- Expert in describing the flow of processes to assist in redesign, reengineering, etc.
- Understanding of the products and services of the business to be able to define the requirements and
- Technical collaboration during the design, development, and implementation of Strategic Business
- Extensive knowledge of business regulations.
- Independently, it solves problems within its area of expertise and/or scales problems to the right staff.
- Applies compliance requirements within its area of responsibility, provides and performs the required
- Understands the lifecycle management of J&J technology.
- Broad understanding of company processes, strategies, and industry trends.
- Intermediate understanding of Johnson & Johnson's IT standards and strategies.
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