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Staff Engineer

hace 3 meses


Juárez, Chihuahua, México Johnson & Johnson A tiempo completo

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
STAFF ENGINEER to be in
CIUDAD JUAREZ.

PURPOSE:


Biosense Webster Inc., a part of the Johnson & Johnson family of companies is currently hiring for a Staff Life Cycle Management Manufacturing Engineer to be in Juarez, Mexico.


Atrial fibrillation (AFIB) is a quivering or irregular heartbeat (arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-related complications.

20 million people around the world suffer from AFIB each year. Biosense Webster, Inc. is the global leader in the science of diagnosing and treating heart rhythm disorders.

The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter.

The introduction of the company's CARTO 3 System in 2009 revolutionized 3D mapping technology by increasing the accuracy, speed, and efficiency of the cardiac ablation procedure.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against based on disability.


Due to ongoing business growth the Staff LCM Engineer will be dedicated to supporting the production lines transfer from Internal to External Manufacturers.

Will be the technical owner of developing and executing to the Equipment and tooling installation and Validation strategies and responsible for the management of the DHF, plus other activities including but not limited to knowledge transfer, transfer of manufacturing documentation and design requirements.


Furthermore, additional responsibilities also include deciding on process changes to meet revised specifications, providing and developing solutions to problems of limited scope, and may provide technical mentorship to lower-level personnel.


YOU WILL BE RESPONSIBLE FOR:

  • Guide the External Manufacturer (EM) on the Validation process, leading the draft and review ofprotocols and test reports.
  • Offers onsite support at the EM during the execution phase of validations (IQ, OQ, PQ).
  • Drafts Validation Strategy and Equipment and Tooling strategies.
  • Review current DHF status for products in scope.
  • Identify needed strategies and inputs from R&D & other functions.
  • Plan and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria while devising new approaches to problems encountered.
  • Plan, schedule, conduct, and coordinate detailed phases of engineering work in part of a major project or in a total project of moderate scope that involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.
  • Additional duties of this role would include updating work instructions, part specifications, validation protocols, technical documents (PFMEA's, ECOs, NCR's, CAPA's), and various forms of reports and correspondence.
  • Applies intensive and diversified knowledge of engineering principles and practices in broad areas of assignments and related fields.
  • Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work.
  • Requires the use of advanced techniques and the modification and extension of theories, precepts and practices of his/her field and related sciences and disciplines.
  • Responsible for one or more of the