About the Company:
| Company: | JOHNSON & JOHNSON |
| Job Role: | SENIOR QUALITY ENGINEER (TERCER TURNO) |
| Experience: | (0 years): |
| Vacancy: | 8 |
| Qualification: | BE/BTech, ME/MTech, MBA |
| Salary: | MX$43,000 /mo |
| Location: | Juarez, Mexico |
| Join us on Telegram | Click Here |
| Apply Mode: | (Online) |
| Start Date: | Not Mentioned |
Job Description:
"Johnson & Johnson companies are equal opportunity employers"
At Johnson & Johnson, the world's largest healthcare company, we come together for one purpose: to transform the history of human health.
Diversity and inclusion are essential to continue to build our history of pioneering and innovation, which has been impacting the health of more than one 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 job openings at the world's largest healthcare company.
When you join Johnson & Johnson, your next move could be our next discovery.
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Some might call this a great inheritance. At Biosense Webster, we say it's just the beginning.
SENIOR QUALITY ENGINEER (THIRD SHIFT)
Summary of the position:
The Senior Quality Engineer plans, conducts and directs engineering projects or studies including complete projects that require advanced knowledge in a specialized field. They apply a broad and diverse knowledge of engineering principles and practices within assigned areas. They can coordinate and direct the activities of technical support staff and are responsible for the technical development of assigned staff The Senior Quality Engineer will use quality engineering tools and practices for the effective and efficient development of transfers and maintenance of products / processes in the entire life cycle of the product. The position holder will also use quality engineering principles and research and problem solving skills to improve and maintain products / processes that are aligned with quality and global business vision. He will use appropriate risk management to prevent unanticipated failure modes and improve process capacity. This person will support the business processes.
Duties and responsibilities:
Under limited supervision and in accordance with all federal, state and local laws / regulations and Johnson & Johnson Corporate procedures and guidelines, this position:
Business Improvements:
Review / analysis of the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and other improvement tools and programs. Conduct benchmarking to develop more effective methods to improve quality. Supports quality engineering development and quality compliance with appropriate skills for new product introduction, and product life cycle management. Reviews and approves engineering change orders (ECOs) Compliance / Regulatory Reviews / analyzes if current products and processes (including actions or decisions carried out) comply with standards, such as QSRs, ISO 13485, etc. including providing support during internal and external audits · Participate in activities to prepare for / or interactions with regulatory agencies (FDA, JJRC, BSI, etc.) Responds to observations from internal or external audits related to the quality engineering function. Establishes and appropriately maintains the required documentation of quality assurance activities and / or quality systems. It carries out periodic audits of the line to evaluate GMPs, production controls, batch segregation and process audits according to JJPS. Review the results of the area audits to ensure that the corrective and preventive actions are adequate.
New Products / Process Introduction :
Works with NPI and the manufacturing, process engineering, and manufacturing engineering departments to develop, conduct, and approve product and process validation strategies.
Product Quality, Control & Disposal and Performance Standards
He directs and attends NCs Review Boards as a member of MRB.
Conduct or support investigations, bounding, documentation, review and approval of nonconformities (NCs), preventive and corrective actions (CAPAs) and customer complaints. Escalation of quality problems as applicable. Support in the analysis of products related to customer complaints to determine failure modes. Responsible and owner of the identification of the material, segregation of materials, classification of the types of defects, including the successful application of these techniques in the day-to-day manufacturing.
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