BlogPublicar vacante
Crea un CV

Buscar empleo

Limpiar filtros

Bolsa de trabajo quimico en validacion de sistemas computarizado Presencial - OCC

2 resultados

Ordenar por: Relevancia

Relevancia

Fecha

Supervisor de Aseguramiento de Calidad para laborar en EUA

Sueldo no mostrado por la empresa

We seek a Quality Assurance/ Quality Control Supervisor (3-5 years of experience) in pharmaceutical manufacturing to join our team. As a QA/QC Supervisor, you will be responsible for ensuring that our ...

  • Vivir y trabajar en EUA
  • Estabilidad laboral
  • Seguro de gastos médicos
Empresa confidencial
Edo. Méx.​

Manufacturing Manager

Sueldo no mostrado por la empresa

MANUFACTURING MANAGER 2A Supply Leader Manufactura Personal Care Manufactura 1. Objetivo del Puesto Asegurar el cumplimiento de los objetivos operativos de la planta en materia de segurid ...

unilever
CDMX
  • 1

Hace 1 día

Supervisor de Aseguramiento de Calidad para laborar en EUA

Si el reclutador te contacta podrás conocer el sueldo

Empresa confidencial

Sobre el empleo

Categoría: Manufactura - Producción - Operación
Subcategoría: Manufactura
Educación mínima requerida: Universitario titulado

Detalles

Contratación:

Permanente

Horario:

Tiempo completo

Espacio de trabajo:

Presencial

Beneficios

  • Vivir y trabajar en EUA
  • Estabilidad laboral
  • Seguro de gastos médicos

Descripción

We seek a Quality Assurance/ Quality Control Supervisor (3-5 years of experience) in pharmaceutical manufacturing to join our team. As a QA/QC Supervisor, you will be responsible for ensuring that our products meet the highest standards of quality and compliance with regulations. You will oversee all aspects of quality management, including analyzing data, implementing quality systems, conducting quality inspections, and performing quality control activities.

 

Duties:

- Develop and implement quality management systems and processes to ensure compliance with CGMP and regulations

- Analyze data and trends to identify areas for improvement in product quality

- Conduct regular quality inspections to ensure adherence to specifications and standards

- Collaborate with cross-functional teams to resolve quality issues and implement corrective actions

- Perform internal audits and lead external audits to assess compliance with quality standards

- Develop and maintain documentation related to quality control procedures, including standard operating procedures (SOPs) and work instructions

- Conducts quality investigations /deviations and reviews corrective action plans for adequacy and compliance. This includes root cause analysis and product impact assessments for investigations resulting from deviations and OOS.

- Ensures appropriate CAPA actions are identified and addressed.

- Approves investigations/CAPAs.

- Train employees on quality control processes and procedures

- Monitor supplier performance and conduct supplier audits as necessary

- Stay up-to-date with industry trends and changes in regulations related to product quality

- Experience with pharmaceutical government agencies regulatory audits

 

Requirements:

- Bachelor's degree in a relevant field, chemistry background, QFB

- Proven experience in quality management, preferably in a manufacturing or pharmaceutical environment

- Strong knowledge of CGMP regulations and regulatory requirements

- Experience with quality inspection techniques and tools

- Excellent analytical skills with the ability to analyze data and identify trends

- Strong attention to detail and accuracy

- Effective communication skills, both written and verbal

- Ability to work collaboratively in a cross-functional team environment

- Strong problem-solving skills and the ability to implement effective corrective actions

- 3 to 5 years of experience in a similar position

- Ability to operate under deadlines while still meeting standards

- Ability to effectively lead, train, supervise, and motivate others to successful completion of goals

- Excellent organizational and time-management skills

- Clear and accurate data entry and documentation skills; strong follow-through and perseverance to handle multiple tasks simultaneously

- Strong competency working with integrated data systems, Microsoft Office Suite, including Outlook and intermediate to advanced Word and Excel (i.e., spreadsheets, formulas, importing and exporting of files, as applicable) as required

- English advanced.

- Willing to relocate to North Texas. We assist with housing.

- Passport and USA Visa

 

 

Job Type: Full-time, Monday through Friday, day shift

 

Pay: According to experience

 

Benefits:

  • Health Insurance
  • Dental Insurance
  • Vision insurance
  • Life insurance
  • Paid Time Off

 

If you are a dedicated professional passionate about ensuring product quality, we invite you to apply for the position of QA/QC Supervisor. Join our team and contribute to our commitment to delivering high-quality products that meet customer expectations. 

Recuerda que ningún reclutador puede pedirte dinero a cambio de una entrevista o un puesto. Asimismo, evita realizar pagos o compartir información financiera con las empresas.

ID: 20377219

También puedes buscar

Químico De Producción

Químico

Químico Analítico

VER MÁS

También puedes buscar

Químico De Producción

Químico Analítico

Químico De Desarrollo

Químico

Quimico De Análisis

Analista Químico

VER MÁS

Refina la ubicación de tu búsqueda

México

Ciudad de México, México

Estado de México, México

Refina la ubicación de tu búsqueda

México

Estado de México, México

Ciudad de México, México

Candidatos
Crea un CV
Inicia sesión
Preguntas frecuentes candidatos
ios
android
Empleos por clasificación
Vacantes por Estado
Vacantes por Ciudad
Vacantes por Categoría
Vacantes más buscadas
Vacantes por Contrato
Vacantes por Empresa
Buscar empleo en México y el mundo
Empresas
Busco talento / Publicar Anuncio
Ayuda para reclutadores
Preguntas frecuentes de reclutadores
OCC
Acerca de OCC
Blog
Trabaja en OCC
Ayuda

OCC D.R. © 1996-2025 Derechos reservados. Versión del sitio candy-serp@