PRINCIPAL ENGINEERING CLERK (TEMPORAL 12 MESES)

At Johnson & Johnson,  we believe health is everything.
Our strength in healthcare innovation empowers us to build a  world where complex diseases are prevented, treated, and cured,  where treatments are smarter and less invasive, and  solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.
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DE&I Statement For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
We are searching for the best talent for PRINCIPAL ENGINEERING CLERK to be in Juárez (INDEPENDENCIA) Purpose.
Provide overall support for engineering activities Provide support during validation activities and writing the documentation.
Responsible for engineering purchases through different purchasing platforms 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.
o Perform NCR lifecycle documentation and investigation, using statistical concepts.
o Provides technical support to identify the causes for non-conformances and process failures and to implement corrections thus assuring process performance and compliance against Ethicon’s QSR, GMP and ISO requirements for the manufacturing process.
o Performs non-conformance investigations including NCR origination, bounding, product control, failure investigation, correction, and documentation with the non-conformance system.
o Support engineers in performing validation activities, execution of protocols, engineering studies and documentation.
o Help to Write engineering documentation (protocols, procedures, special instructions, reports, etc.) o Supports the documentation changes in compliance with Ethicon’s Change management system.
o Engineering support in the completion of projects mainly focused on quality improvements, cost/scrap reduction, increased capacity and New Products.
o Conduct robust investigations.
Analyzes data and recommends actions for process, equipment and system improvement.
o Ensure compliance to the quality policy in all activities.
o Ensure safe working conditions and practices in the department as well as providing support on the plan safety requirements.
o Enable proactive approach for process performance and customer satisfaction driving appropriate actions across all levels of the organization.
o Acts in accordance with safety regulations and procedures.
o Supports internal and external audits and inspections.
o Submit purchase requisitions for Engineering department.
o Support Project Spending Management.
o Other responsibilities may be assigned and not all responsibilities listed may be assigned.
o Responsible for communicating business related issues or opportunities to next management level o Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
o 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 o Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
o Performs other duties assigned as needed.
Qualifications REQUIREMENTS.
A minimum of High School Diploma and Engineering Bachelor’s Degree complete or in progress.
From 6 to 8 years of experience in related fields.
Or currently pursuing an Engineering Bachelor’s Degree with half of School credits completion or recently completed Bilingual English/Spanish (Preferred).
Computer skills.
Excel (including charts/graphs), Word, Internet Explorer.
Experience in medical device manufacturing environment.
(Preferred) Knowledge on medical product and process design concepts such development, materials, standardization science and basic statistics.
(Preferred) Knowledge of word processing, spreadsheet analysis, presentation graphics, some engineering analysis and some statistical software (Minitab preferred).
Analytical thinking to provide and lead product inquiry investigations.
Ability to work in cross-functional team to complete projects, knowledge in PE tools such as Kaizen Ability to solve basic problems using FI methodologies such as Five Whys, 5Ms, and others.
Self-motivated Strong communication and interpersonal skills.
Requires good networking.
Entails significant interaction with technical peers and manufacturing associates.
Self-motivated and capable of completing job duties with limited supervision