Quality Director

hace 1 mes


Nuevo Laredo, Tamaulipas, México Medline Industries, LP A tiempo completo

Position Overview

Medline Industries, LP is seeking a qualified Director de Calidad to lead the development of product specifications for Medline branded products. This role involves directing the development of testing requirements, procedures, and methods for testing, inspecting, or qualifying new products and suppliers.

Responsibilities

The Director de Calidad will partner with the Supplier Audit department and Division to determine optimal Supplier relationships. This role also involves developing and implementing strategy for the Quality department(s) based upon Quarterly Management Review.

Key Accountabilities

Direct the development of product specifications for Medline branded products, including testing requirements, procedures, and methods for testing, inspecting, or qualifying new products and suppliers.Partner with the Supplier Audit department and Division to determine optimal Supplier relationships.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 develop; 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.

Requirements

  • Typically requires a 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.
  • Depth of technical knowledge of relevant standards and regulations (21CFR 820, ISO 13485, ISO 14971, MDSAP, and MDR).
  • Proficiency in analyzing and reporting data to identify issues, trends, or exceptions to drive improvement of results and find solutions.
  • Demonstrated ability to control and coordinate concurrent projects, competing priorities, and critical deadlines.
  • Advanced level skill in Microsoft Excel (for example: using AVERAGE function, merging and centering cells, printing centered page and/or creating a pivot table).
  • Position requires travel up to 30% of the time for business purposes (within state, out of state, and/or internationally).

Preferred Qualifications

  • At least 6 years of managerial experience preferred.
  • At least 8 years of related experience in Medical Device, Pharmaceutical, Food, Cosmetic, or Personal Products industries preferred.

Equal Opportunity Employer

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status, or any other legally protected characteristic.



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