PRINCIPAL PROJECT TECHNICIAN (SEGUNDO TURNO)
at Johnson Johnson
Ciudad Juárez, Chih., Mexico -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Nov, 2024 | Not Specified | 29 Aug, 2024 | 6 year(s) or above | Statistical Analysis Tools,Mechatronics,English,Documentation,Mechanics | No | No |
Required Visa Status:
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US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
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.jnj.com/.
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 PRINCIPAL PROJECT TECHNICIAN (SEGUNDO TURNO) to be in Juarez, Chih., in Plant Salvarcar.
Independently, or under limited or null supervision, works on complex by nature assignments, which require considerable criteria, judgment, and initiative to solve problems and issue recommendations. 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 and follows up in quality and regulatory requirements comprehended in the business strategy. keeping the expected levels of the Department in the GMPs (Good Manufacturing Practices). Compliance with the Good Manufa cturing Practices (GMPs) making observations and communicating them to his/her supervisor for their correction.
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:
- Identifies, designs, and develops the necessary equipment.
- Performs material tests.
- Studies the processes to implement improvements.
- Responsible for preparing and managing specifications.
- Responsible for purchasing and designing equipment and tools that meet manufacturing, safety, and environment requirements.
- Participates in saving and capital projects.
- Responsible of complying with finance metrics
- Responsible for evaluating and developing action plans for quality, safety, cost, service, and regulatory compliance requirements.
- Performs activities of process/product validation.
- Follows the Convenient Information Retention Administration Policies of J&J and of the Campus, record retention program, training and education, Document Retention Notices, Record cleanup, inactive records and Information Management, Vital Records, and if applicable, to suppliers. Performed other duties.
- 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
Requirements:
- Vocational, Certificate, Technical or Associates, minimum a technical career, applicable to mechanics, mechatronics.
- Generally, requires 6-8 years’ work experience related to the position or equivalent, preferably.
- Preferably knowledge in medical Industry
- Knowledge of good manufacturing practices and documentation, preferably in the medical industry.
- Experiment design
- Knowledge in statistical analysis tools
- Management of statistical procedures.
- Knowledge of computer programs.
- Oral and written communication in Spanish and English
- Advance English, preferably
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:6.0Max:8.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Trade Certificate
Vocational certificate technical or associates minimum a technical career applicable to mechanics mechatronics.
Proficient
1
Ciudad Juárez, Chih., Mexico