Résumé des fonctions
This position is responsible for directing the operation of a well-integrated and optimized manufacturing unit that fosters high quality, compliance with all regulatory requirements, and cost efficiency.
Responsible for implementing local manufacturing strategy that is integrated with Zimmer Biomet marketing and growth plans, as well overseeing all manufacturing operations and engineering activities related to the production of Zimmer Biomet products.
Devoirs et responsabilités principales
Implement local manufacturing strategy that is integrated with Zimmer Biomet marketing and growth plans. · Oversee all manufacturing operations and engineering activities related to the production of Zimmer Biomet products.
Drive and link business opportunities with the application of innovative technologies in manufacturing processes. · Predict and redesign manufacturing systems to bring about dramatic improvements in performance while still complying with current and future regulations.
Interface with Product Development, Franchise Management and Marketing groups for successful introduction of new products.
Attract, retain, and encourage individual development of key personnel for future assignments by arranging appropriate formal training, mentoring, or other experiences.
Develop and drive an operating culture that promotes consistency of behaviors that lead to superior business performance.
Lead, manage, and communicate effectively.
This is not an exhaustive list of duties or functions
Domaines de compétence attendus
Experience with manufacturing technologies used in the orthopedic and or dental implant industry is preferred.
Experience guiding and implementing high velocity large scale change initiatives that produce greater level of innovation, quality, service, efficiency, and learning.
Demonstrated ability to partner with logistics, sourcing, R&D and other internal functions with proven record of successful negotiations and problem resolutions.
Ability to effectively lead a team in the achievement of objectives. Understanding of applicable legal and regulatory requirements within the medical device industry.
Excellent written and oral communication skills and problem solving skills are essential. Must have proficiency and experience in the following areas : capacity planning and development;
budgeting for multiple profit centers; development of quality / productivity plans; new product process development; manufacturing flow analysis and implementation, personnel selection, management, and development.
Formation / Expérience requise
Bachelor’s Degree in an applicable engineering or business discipline 10 years of progressive and extensive applicable work experience in manufacturing, quality, or development engineering of which 5 years + supervisory experience Strong communication, leadership and organizational skills are essential as well as a full understanding of the manufacturing process.