Senior Manager, Third Party Manufacturing (all genders) - permanent fulltime

Senior Manager, Third Party Manufacturing (all genders) - permanent fulltime Full-time Workday Global Grade: 19 Company Description What makes you stand out, makes you ready to make an impact. At AbbVie Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You’ve come to the right place! Job Description AbbVie is seeking a Senior Manager, External Manufacturing to lead the relationship with and performance of its third-party manufacturers. In this strategic and operational role, you will serve as AbbVie's primary point of contact for several industrial partners. You will directly contribute to ensuring continuity of supply, quality, regulatory compliance, manufacturing performance, and cost competitiveness for externally manufactured products. This opportunity is suited to someone who wants to grow within a multicultural organization that combines agility, commitment, and speed of execution. Key responsibilities Manage relationships with third-party manufacturers by defining effective governance, responsibilities, operating models, and communication channels. Ensure continuity of supply by coordinating forecasts, production schedules, and delivery plans with Supply Chain, Planning, and industrial partners. Anticipate and manage operational risks related to capacity, raw materials, components, lead times, or supplier performance to prevent supply disruptions. Lead governance and operational performance through Virtual Operations Teams (VOTs), business reviews, and steering committees with third-party manufacturers. Define, monitor, and improve performance indicators covering quality, service, cost, capacity, and lead times, and coordinate the associated action plans. Drive issue resolution and required escalations, preparing reports and executive summaries for management. Ensure compliance with quality and regulatory requirements in close collaboration with Quality teams and manufacturing partners. Coordinate audits, inspections, annual quality reviews, deviations, investigations, and CAPAs, ensuring corrective actions are implemented within expected timelines. Contribute to product release and decision-making regarding potential non-conformities. Lead technology transfers and strategic projects related to external manufacturing, process changes, and manufacturing performance improvement. Coordinate internal teams and industrial partners throughout projects, managing risks, timelines, resources, costs, and communication. Support products throughout their lifecycle and identify opportunities to improve reliability, manufacturing robustness, and profitability. Qualifications You bring: Degree in Engineering or a scientific discipline Minimum 7 years of experience in the pharmaceutical, biotechnology, or related regulated industry Sterile manufacturing experience (mandatory) Aseptic processing experience (mandatory) Technology transfer experience (mandatory) Strong project management and supplier management skills Excellent stakeholder management, negotiation, and communication capabilities GMP and quality systems knowledge Willingness to travel for business approximately one-third of the time. Additional Information Here's how we can move mountains together: with a diverse work environment where you can have a real impact with an open corporate culture with an attractive salary with an intensive onboarding process with a mentor at your side with flexible work models for a healthy work-life balance with a corporate health management that offers comprehensive health and