Quality Engineer Ii (Temporal 12 Meses) - Ciudad Juarez

Quality Engineer Ii (Temporal 12 Meses) - Ciudad Juarez
Empresa:

Johnson & Johnson


Lugar:

Chihuahua


Área:

Otros

Quality Engineer Ii (Temporal 12 Meses) - Ciudad Juarez

Detalles de la oferta

"Johnson & Johnson companies are equal opportunity employers" Company:Ethicon Endo-Surgery develops and markets advanced medical devices for minimally invasive and open surgical procedures, focusing on procedure-enabling devices for the interventional diagnosis and treatment of conditions in general and bariatric surgery, as well as gastrointestinal health, gynecology and surgical oncology. More information can be found at the new company website www.ethiconendosurgery.com. Searching the best talent for:QUALITY ENGINEER IIMain responsibilities:• Monitor all FGQA quality assurance functions• Establish and maintain appropriate documentation as required for Quality Assurance activities and the Quality Documentation Systems• Develop statistical sampling plans and perform process capability studies• Implement process control systems and provide technical support for process validations• Provide QS support in Product transfers and new products development• Assist in training new engineers, train technicians and supervisors in process changes• Perform Complaint analysis investigation as needed• Participate in process/ quality improvement projects• Assist with implementation of EES applications for quality systems• Support COGs initiatives• Responsible for following and administering safety• Compliance with safety policies and procedures• Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third party vendor if applicable.• Follow J&J and EES Records Management Policies for Convenience Information, Records Retention Schedules, Training and Education, Document Hold Notices, Records Cleanout, Inactive Records and Information Management, Vital Records and third party vendor if applicable.• Assist, review & approve non-conformances investigations & non-conforming product dispositions.• Provide as needed, subject matter expert feedback on manufacturing process changes.• Other responsibilities may be assigned and not all responsibilities listed may be assignedReporting to: BUSINESS UNIT QUALITY MANAGER
Qualifications
Requirements and Education: • Bachelor degree in engineering- mechanical, electrical, industrial, preferred or Applicable science or business degree• CQE, CRE, CQA 2– Ratings, **GB preferred.• ASQ Quality Engineering/ Auditor Certification preferred • 2 - 4 years related work experience, or demonstrated performanceKEY SKILL / KNOWLEDGE REQUIREMENTS:SKILL SETS:• Bilingual: English/ Spanish preferred• GMP/ ISO knowledge preferredCOMPUTER SKILLS:• PC experienceGlobal Leadership Profile Competencies Integrity and Credo-based Actions ~ lives Credo values; builds trust; tells the truth; initiates transparency into problems; demonstrates genuine caring for peopleCollaboration and Teaming ~ puts interests of enterprise above own; works well across functions and groups; builds teams effectively; inspires follower ship; instills a global mindsetResults and Performance Driven ~ assumes personal ownership and accountability for business results and solutions; willing to make tough calls; consistently delivers results that meet or exceed expectations; demonstrates a track record of people development; champions diversity; net exporter of successful talent.Sense of Urgency ~ proactively senses and responds to problems and opportunities; works to reduce "cycle" time; takes action when needed


Fuente: Neuvoo_Ppc


Área:

  • Otros / Otros

Requisitos

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