Quality Director
hace 1 mes
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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