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Quality Engineering Manager

Quality Engineering Manager
Empresa:

Abbott Laboratories


Lugar:

Caguas

Detalles de la oferta

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 103,000 colleagues serve people in more than 160 countries. This is a pipeline requisition to connect with talents for future opportunities in our Structural Heart manufacturing business located in Caguas, Puerto Rico. HAVE YOU EVER DREAM OF MAKING AN IMPACT ON THE WORLD? How? Become a Quality Engineering Manager in our Structural Heart manufacturing business located in Caguas, Puerto Rico. As a Quality Engineering Manager you will be r esponsibile for planning, implementation and control of quality control procedures to support the actual company QA system and to facilitate technology transfer to the site. This position will proactively lead and coach Quality Engineering and Supplier Quality Engineering resources, actively participate in site activities as part of the Quality Management Team and lead the Quality/Supplier Engineering organization by envisioning short and long-term goals, overcoming intra-facility barriers to success, and energizing the facility to become a quality driven organization. HOW WILL YOU MAKE A DIFFERENCE? Supervises the QE staff to ensure adherence to facility QE systems. Responsible for providing functional guidance to technical staff within the Quality Department and for their development. Recommends and implements modifications to improve QA system efficiency and develops new analytical methods and techniques. Assist quality improvement team members by identifying problems, examining solution options, implementing action plans, and providing resources to teams as needed. This responsibility includes driving improvements in key quality indicators/systems such as yields, quality incidents/escapes, and complaints/FER. Responsible for process validation from the quality perspective and quality compliance for all products produced in the facility. Coordinates investigation, reporting and implementation of required corrective and preventive actions in any documentation, inspection and release functions nonconformance. In conjunction with operations and engineering personnel, establishes requirements for the transfer of technology/methodology facility. Ensure compliance with all procedures and all applicable regulatory agency requirements. Other duties as assigned CAN’T WAIT TO GET STARTED? To be successful in this role, you will require the following qualifications: Bachelor degree in engineering is required. Certifications in Lean or Six Sigma are a plus. 7 years of experience in Quality as well as Materials and/or Operational Management is required. Experience in the medical device, pharmaceutical, bio-medical or electronic industry is preferred. 4 years of experience at a supervisory/managerial level is required. Requires the ability to change the thinking of, or gain acceptance of, others in sensitive situations. Comprehensive verbal and written analytical/problem solving, communication, negotiation, interpersonal, training and presentation skills are essential. Must have demonstrated knowledge / experience in process validation, regulatory compliance, and people management. Must be knowledgeable of GMP and ISO evidenced by successful completion of training in GMP, auditing principles, and process validation. Must have good verbal and written communication in English and Spanish.


Fuente: Adzuna_Ppc

Requisitos

Quality Engineering Manager
Empresa:

Abbott Laboratories


Lugar:

Caguas

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