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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.
The Global Job Posting policy promotes the dedication to the advancement and development of our employees. We invite you to read this posting and apply if you are passionate about the position and meet the requirements.
The Global Job Posting policy promotes the commitment to the advancement and development of our employees. We invite you to read this posting and apply if you are interested in the position and meet the requirements.
Biosense Webster, Inc. is recognized worldwide as a leader in the science behind the diagnosis and treatment of cardiac arrhythmias. We help patients around the world regain their health, their energy and their lives. Guided by the needs of electrophysiologists and cardiologists, Biosense Webster, Inc. has pioneered innovative technological advancements for more than 30 years. Join us as we continue to look for new and better ways to help physicians heal more hearts. Because that is what we do - we put lives back in rhythm.
Searching the best talent for: SENIOR PROCESS ENGINEER
Reports to the Engineering Manager, identifies and develops internal areas of opportunities through the DMAIIC methodology and tools of Excellency in processes with the purpose of reducing the manufacturing cost of the products and continue with the culture of continuous improvement comprehended in the strategy of BWI.
DUTIES & RESPONSIBILITIES
Under (e.g. limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
Identifies, designs and develops the necessary equipment.
Performs material tests.
Studies the processes to implement improvements.
Responsible for preparing and managing specifications.
Assists technicians and engineers about unusual problems.
Responsible for purchasing and designing equipment that meets safety and environment requirements.
Performs activities of process/product validation.
RESPONSIBILITIES OF SUPERVISION ENGINEERS 1 AND 2: Can supervise, coordinate and technically revise the work of a limited group of technicians.
Responsible for communicating business related issues or opportunities to next management level
Responsible for ensuring 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
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
Performs other duties assigned as needed
Masters or Doctorate in Science or Engineering, preferably.
Bilingual (English-Spanish), preferably
Trained to have technicians under his charge.
4 to 6 years of experience in a product development and/or manufacturing
environment or equivalent experience. Experience in the medical product
industry is preferable.
REQUIRED KNOWLEDGE, SKILLS, ABILITIES and CERTIFICATIONS/LICENSES:
To possess abilities in group dynamics, ability to work multifunctionally and obtain collaboration among multiple
Effective communication skills, written, spoken and in presentation.
Ability to manage projects, lead teams in different places performing projects.
Technical competences, preferably
o Tool design
o Product/process risk assessment
o Cleaning validation
o Equipment design and automatization
o Interplant transfers
o Test methods development and validation
o Lean and Six Sigma skills
o Process validation
o Design validation and verification
o Operations direction
o Process technical writing
o Regulations knowledge
o Plastic injection molding
Technical skills, preferably:
o Plastic processing
o Mechanical and electrical skills
o Process characterization
o Geometric Dimensions and Tolerances (GD&T)
o FEA (Finite Element Analysis)
o Knowledge of polymers
o Chemical processing
o Electrical, electronic and PLC
o DFMA (Manufacturing and Assembly Design)
o Development of the assembly and equipment process
o Calibrators development and metrology
o PLC (troubleshooting)
Knowledge of operations, products and processes of the company, preferably.
Knowledge of the Quality system of the company.
Knowledge of GMP/ISO, preferably
o Efficiency in word processing programs, spreadsheets, presentations and database applications.
o Statistical analysis software
o Engineering applications software (FEA, CAD, etc.), when required.
ADDITIONAL POSITION REQUIREMENTS
Requires to work in an office environment and/or in a Controlled Manufacturing environment.
RESPONSIBILITY FOR OTHERS (If applicable)
This position reports to Engineering Manager.
PHYSICAL WORKING CONDITIONS / REQUIREMENTS
This position will perform in an office and in a clean room production controlled environment and office areas.
Must be capable of standing for moderate periods of time and sit on a desk in front of a computer.
Regular use of office tools necessary to perform the duties and responsibilities of the position.
Cordis de Mexico S.A. de C.V. (8286)