Quality Director

hace 1 mes


baja california, México Medline A tiempo completo

Descripción y detalle de las actividades

Responsibilities:

  • Direct the development of product specifications for Medline branded products, such as the testing requirements, procedures and methods for testing, inspecting or qualifying new products and suppliers.
  • Partner with Supplier Audit department and Division to determine optimal Supplier relationship.
  • Develop and implement strategy for the Quality department(s) based upon Quarterly Management Review.
  • Prepare and deliver Customer presentations.
  • Act as liaison with Senior Leadership of Divisions, Suppliers, Manufacturing, and/or Operations to ensure quality products, on time delivery, and customer satisfaction.
  • Collaborate with Suppliers, manufacturing partners and product managers in developing and implementing QA programs.
  • Oversee QSR for assigned department(s) and ensure compliance as measured by FDA/ISO/internal audits.
  • Management responsibilities include:
  • Typically, manages through multiple Managers.
  • Provides leadership and management to one or more major departments of an operating unit or to a department that has system-wide accountability.
  • Strategic, tactical and operational planning (12 + months) for the function or department.
  • Direct budgetary responsibility for one or more departments, functions or major projects/programs.
  • Interpret and execute policies for departments/projects and develops; Recommend and implement new policies or modifications to existing policies; Hiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies.


Experiencia y requisitos

  • Bachelor’s degree in Engineering, Science, or Technical Field.
  • At least 7 years of experience related to the design/operation of medical device or drug combination product platforms, design controls, risk management, including working in compliance with QSR/GMP/ISO requirements or other regulated industries (21CFR 820, ISO 13485, ISO 14971, MDSAP, and MDR).
  • At least 4 years of management experience.


Beneficios

  • Beneficios de acuerdo a la LFT

Número de vacantes 1

Área Calidad

Contrato Permanente

Modalidad Presencial

Turno Diurno

Jornada Tiempo Completo

Salario mensual neto $1,000 - $2,000 MXN

Estudios Carrera con título profesional

Inglés Hablado: Avanzado, Escrito: Avanzado

Disponibilidad p. viajar Si

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