
Sr. Associate, QA Compliance
Descripción general
Aquí es donde usted marca la diferencia en la seguridad de nuestros pacientes. Como miembro del equipo de Calidad de Baxter, desempeñará un papel esencial en nuestra misión de salvar y sostener vidas. La calidad es importante durante todo el ciclo de vida del producto y trabaja en colaboración con todas las áreas de la organización. Debido a que Calidad afecta todo lo que hace Baxter, un rol en Calidad brinda muchas oportunidades de crecimiento, aprendizaje y una carrera exitosa que tiene un impacto diario en la vida de las personas.
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Apoyo a las padres
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Educación continua/ Desarrollo profesional
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Salud de los empleados y Beneficios de bienestar
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Tiempo libre pagado
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2 días al año para ser voluntario
Perfil de éxito
¿Qué hace que un miembro del equipo de calidad de Baxter sea exitoso? Revise algunos de los rasgos principales que estamos buscando y vea si su perfil se ajusta.
- Orientado al detalle
- Aprendiz continuo
- Valiente
- Colaborativo
- Pensador crítico
- Influyente
Sr. Associate, QA Compliance
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.
Sr, Spec, Quality - Compliance
To perform internal quality audits to ensure the compliance to all systems and
procedures and ulmately build the quality focused and ensure appropriate CAPA is
placed.
To ensure that system and facilies comply as per the regulatory requirements and
expectaons.
To ensure cGMP compliance status of site as per regulatory requirements.
To ensure and sustain all me ready plant in line with current regulatory expectaons for
regulatory authories and other partner inspecon.
To verify process and systems are complying standard operang procedures (SOPs) and
current regulatory requirements and expectaons.
To ensure that audit observaon compliance and effecveness of CAPA.
To perform external audit related process.
To perform GEMBA round of site and report in case of any non-conformance observed
during round.
To perform periodic assessment of the GMP trends.
To perform the assessment of regulatory intelligence program and global observaon
cerficaon.
To ensure that the required inial and connuing training of personnel is carried out and
adapted according to need.
To impart training to personnel regarding enhancement in regulatory guidelines, system,
and processes.
To handle electronic QMS modules for review and approval of changes, procedures etc.
To ensure that data integrity is being maintained at all level and to perform / get performed
regular checks to ensure that system is in state of control.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
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.
Dirección

Chacharvadi Vasna
Ahmedabad- 382213
Gujarat
India Explorar esta ubicación
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