Associate Director Manufacturing Science & Technology - Tapi Montà

Associate Director Manufacturing Science & Technology - Tapi
Montà
Piemonte, Montà

Associate Director Manufacturing Science & Technology - TAPI Date: Jan 17, 2025 Location: Santhia, Italy, 0000 Job Id: 60210 TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products, we are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. Our reliable history in the generic API industry dates back over 80 years, and we are considered one of the most trusted API suppliers, enabling TAPI to lead the industry based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. TAPI employs more than 4, 000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. Main responsibilities and activities In the Manufacturing Science & Technology Department, we are looking for a brilliant profile reporting to the Site General Manager with the following responsibilities and activities: Leads the MS&T group on the Santhià site, ensuring necessary technical and scientific support to the manufacturing activities of commercial products aimed at process improvement and problem solving. Collaborates with other company functions to ensure the effective management of product manufacturing processes. Collaborates with the Research and Development function to ensure robust industrialization/scaling, validation, and reliability during the development phase of new product manufacturing processes. Participates with other business functions in the change management process ensuring that all changes to processes and technologies used in the manufacturing processes of commercial products or the introduction of new processes/technologies are carried out in line with company procedures and in accordance with cGMP requirements. Supports other company functions in the event of anomalies or deviations in the manufacturing processes of commercial products, ensuring technical and scientific support. Leads strategies for line optimization, cost reduction, competitiveness improvements, new product introduction, and transfer in/out projects. Translates the site's plan on mentioned projects/initiatives to a detailed production schedule in close cooperation with Site SC. Ensures workflow optimization and implements processes for manufacturing new products. Understands changes in business needs and transfers them into strategy. Ensures quality of all manufactured products and maintains environmental regulations and standards. Ensures knowledge of TAPI's strategy, direction, and challenges. Familiarizes with competition, industry trends, and technologies to recommend creative and innovative solutions. Participates in global project groups. Proactively shares best practices, process improvements, and lessons learned across the TAPI Network. Executes product transfers and material changes under function responsibilities. Looks after the wellbeing, safety, and health of the workforce. Ensures employee engagement and motivation to function successfully by fostering a team-based and caring environment and by being visible to all staff. Drives employee enablement and ensures proper training is provided to guarantee certified, competent staff to accomplish the required tasks. Leads the MS&T management team, tracks performance, and develops talent. Is an influential member of the site management team. Takes an active role in promoting cross-site initiatives, teamwork, and collaboration across site's functions. Requirements Education: Chemistry/Engineering or equivalent; PhD is preferred. Ensures Quality Management System is fully in place where applicable in the function and within the area of responsibility maintaining total compliance to current GMP, GDP, Data Integrity requirements. Ensures adherence to environment, health, and safety company requirements as well as legal obligations. Behaves according to company Ethical Code and company values. At least 2 years of experience in the role. Strong communication skills, top down and bottom up. Fluent in Italian and English, both written and spoken. What we offer? We try to take care of our employees, offering them small and large benefits. By way of example: Canteen Company Car Working flexibility for Caregivers and parents Coffee Key Recognition Program Welfare Platform Health agreement with medical centers of excellence Up to 2 days home office per week Highly inclusive and multicultural working environment Continuous learning and development programs (with full access to LinkedIn Learning) Type of contract: long-term contract Teva's commitment to equal opportunities Teva is committed to equal opportunities in the world of work. Our global policy requires equal employment opportunities to be provided regardless of age, race, religion, health, identity, gender expression, protected categories, or any other legally recognized status that is entitled to protection under applicable laws. J-18808-Ljbffr