SPEC, QUALITY
Descripción de la oferta de empleo
No importa tu rol en Baxter, tu trabajo tiene un impacto positivo en la gente alrededor del mundo.
Sentirá un propósito en toda la organización, ya que sabemos que nuestro trabajo mejora los resultados para millones de pacientes.
Los productos y terapias de Baxter se encuentran en casi cada hospital del mundo, el clínicas y en los hogares.
Por más de 85 años hemos sido pioneros en innovaciones médicas significativas que transforman el cuidado en salud.
Juntos creamos un lugar donde somos felices, exitosos y nos inspiramos mutuamente.
Aquí es donde puedes hacer tu mejor trabajo.
Únete a nosotros en la intersección de salvar y sostener vidas-donde tu propósito acelera nuestra misión.
This is where you save and sustain lives At Baxter, we are deeply connected by our mission.
No matter your role at Baxter, your work makes a positive impact on people around the world.
You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home.
For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other.
This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
What you'll be doing Ensure compliance with QSR part 820, ISO- and other applicable regulations.
Implements, monitors, improves and reports on metrics to monitor Quality performance.
Ensure that the non-conforming material process is executed in accordance with established procedures and in compliance with determined metrics.
Leads/oversees validation activities, IQs, TMVs, OQs, PQs, for designated areas Ensures that the validated status is maintained during any decision-making process.
Leads or participates in NCR, SNCR, CAPA activities in accordance with established procedures and ensures compliance with quality objectives.
Assists management and departmental staff in the implementation of statistical quality control techniques in order to improve operational efficiency and effectiveness.
esponsible for the analysis of data obtained from the field to investigate and resolve issues identified through Post Market Surveillance Report.
Participates or leads project transfer, through the identification and closing of gaps from the quality system and manufacturing processes, establishing product acceptance criteria, ensuring quality controls and supporting project deadlinesParticipate in Value Stream projects (quality improvements, cost savings, productivity gains).
Ensure that all inspection and test specifications are properly performed and documented.
Conduct a root cause analysis to prevent recurrence.
Supervise that all personnel reporting to him/her are adequately trained for the functions they perform.
Conducts routinary internal audits, Gembas, LTTs of the quality system in compliance with procedures.
Reports audit results to management.
Supervise and coordinate the function of the Quality Technicians, Quality Intern and Quality Eng C.
Ensures compliance with assigned KPIs and notifies management of any possible impact Ensures that subordinates' duties and responsibilities are clearly defined and that performance is routinely measured and reviewed.
This includes.
Definition of performance standards and related objectives; Measurable work standards Evaluating performance to ensure achievement of individual and departmental objectives, using corporate appraisal procedures.
Communicate actual performance against the standard to subordinates, reporting results to management.
Develop key people to ensure smooth operation.
Creates and establishes development plans to build high performing teams Supports analysis, investigation and field actions.
Creates consignees list and contacts clients to obtain required information.
Creates, monitors and ensures compliance with quality plans.
What you'll bring Excellent verbal and written communication skills (English/Spanish) Bachelor's degree Personnel Management Training - Knowledge on risk management ISO QSR Part 820 Training / Awareness and ISO Root cause Analysis Formal education or training in quality control techniques, including quality system audits, statistical tools, design of experiments, statistical sampling methods and testing methods, Lean principles, etc.
(Deseable) Desired Knowledge in medical device regulations and standards, including FDA medical device regulations covered by Title 21 CFR Part 820, European Medical Device Directive /EEC / EU MDR Quality Eng certified by ASQ (Deseable) Green Belt Six Sigma Certified.
(Deseable) Five years in similar positions Problem Solving Focused on Results Validation Expirience (IQ, TMVs OQ, PQ,) Adaptaciones razonables Baxter está comprometida para trabajar y proveer ajustes razonables para personas con discapacidades, a nivel global.
Si por una condición médica o discapacidad, necesitas algún ajuste en cualquier etapa del proceso de aplicación o entrevista, por favor ingresa a este enlace y déjanos saber la naturaleza de tu requerimiento junto a tu información de contacto.
Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information.
To learn how you can protect yourself, review our Recruitment Fraud Notice.
Our products and therapies touch the lives of millions of people around the world every day, which is why we are focused on transformative innovations that bring smarter, more personalized care to all of us.
For 87 years and counting, we have been at the critical intersection where the ideas that save and sustain lives meet the providers who make it all happen.
And now, we are determined to realize our boldest opportunities to transform global healthcare for years to come.
Detalles de la oferta
- 190 Welch Allyn de Mexico, S. de R.l. de C.V. MEX
- Sin especificar
- 13/12/2024
- 13/03/2025
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