Senior Quality Director

hace 3 semanas


Reynosa, Tamaulipas, México ConvaTec Inc. A tiempo completo

Transforming Lives Through Quality Excellence

About ConvaTec Inc.

We are a global medical products and technologies company, pioneering trusted solutions to improve lives. Our focus is on managing chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With over 10,000 colleagues worldwide, we provide our products and services in almost 100 countries, united by a promise to be forever caring.

Our mission is to deliver a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. We are committed to excellence, aiming for nothing short of it. Join us as our Senior Quality Director and contribute to this vision.

About the Role

This senior position is responsible for administrating the Local and Corporate Quality Management Systems and Strategies at the Infusion Care manufacturing site(s) in Mexico. You will ensure customer satisfaction and loyalty through the production and distribution of the highest quality products.

  • You will lead the Quality Management organization at the ID Reynosa Unomedical/ConvaTec Group manufacturing site.
  • As an expert in operation quality systems, you will be sought out by others for guidance and advice.
  • You will develop, communicate, and execute plant Quality Management strategies and visions that align with the Unomedical/ConvaTec Group business objectives.
  • You will anticipate, assess, and manage current and future compliance and process risks, focusing on impact to business success.

Your key responsibilities include:

  1. Developing and managing the local plant Quality budgets, meeting all annual budgetary targets.
  2. Implementing local quality processes, strategies, and resources in the manufacturing site of responsibility.
  3. Ensuring constant state of quality system inspection readiness through proactive work with regional and local partners.
  4. Maintaining an uncompromising commitment to quality and continuous improvement, focusing on meeting customer needs throughout the product life cycle.

You will work closely with regional Operations and sites, as well as partner with Operations to execute and facilitate network initiatives in pursuit of business objectives and targets.

Requirements

To succeed in this role, you will need:

  • Strong experience in a QC/QA leadership role (manager), with at least 5 years in the medical device and/or pharmaceutical manufacturing focus.
  • Practical experience and global mastery in global quality standards and regulations governing medical products, including CFR 820 regulation.
  • Ability to think clearly and decisively, remaining calm under challenging conditions.
  • Ability to efficiently work through quality, organization, and business issues with a focus on solutions and proactive contingency planning.

You must also possess:

  • A minimum of B.S., or equivalent, in a scientific/technical discipline.
  • Certifications in Quality Management Systems, such as ISO 9001 Lead auditor, ASQ Certified Quality Manager, etc.
  • Six Sigma Green Belt Certified (Black Belt preferred).

This role requires around 5% travel.



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