Global Quality Director
hace 1 semana
Rhian_Convatec is a global medical products and technologies company, committed to improving the lives of individuals around the world. As a pioneer in trusted medical solutions, we strive for excellence in our advanced wound care, ostomy care, continence care, and infusion care products.
Our organization operates with a strong focus on innovation, aiming to provide patients with better outcomes and reduced care costs. We are united by a promise to be forever caring and have a presence in almost 100 countries, serving over 10,000 colleagues.
In 2023, Rhian_Convatec achieved revenues exceeding $2 billion, solidifying its position as a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about us, please visit our website.
We are transforming our business for the better, driving the development of better products, working methods, and customer service. Join us on our journey to #ForeverCaring as our Site Quality Director, where you will play a pivotal role in achieving this vision.
About the RoleThis position is responsible for overseeing the Local and Corporate Quality Management Systems and Strategies at the Infusion Care manufacturing site(s) in Reynosa Mexico. The successful candidate will ensure customer satisfaction and loyalty through the production and distribution of high-quality products.
- The Global Quality Director will be accountable for administering the quality management organization at the ID Reynosa Unomedical/Convatec Group manufacturing site.
- As an expert in operation quality systems, they will be sought out by others for guidance and advice.
- They will develop, communicate, and execute plant Quality Management strategies and visions aligned with the Unomedical/Convatec Group business objectives.
The Global Quality Director will:
- Continuously anticipate, assess, and manage current and future compliance and process risks.
- Be responsible for developing and managing the local plant Quality budgets, meeting all annual budgetary targets.
- Drive the implementation of local quality processes, strategies, and resources in the manufacturing site of responsibility.
The ideal candidate should possess:
- Strong experience in a QC/QA leadership role, preferably in the medical device and/or pharmaceutical manufacturing industry, with at least 5 years of experience.
- Practical experience and global mastery in global quality standards and regulations governing medical products, including knowledge of CFR 820 regulation.
The estimated annual salary for this position ranges from $120,000 to $180,000, depending on location and experience.
BenefitsWe offer a comprehensive compensation package, including health insurance, retirement plans, and paid time off.
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