Technology & Innovation Lead, Process Equipment DP (f/m/d)

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: Champion the transformation of process and manufacturing technologies for Takeda’s Drug Product ( D P ) network by setting technical direction, building technology visions and strategies, and enabling scalable execution. Provide specialist process, plant and reliability engineering expertise to ensure safe, environmentally sustainable, reliable, cost-effective, and scalable technical solutions for D P manufacturing plants. Translate site and network needs into harmonized best practices, standards, and roadmaps, ensuring solutions meet Regulatory, Quality, Capacity, and EHS requirements. Accelerate innovation by combining industry benchmarking/scouting with structured deployment approaches aligned to modern digitalization/Pharma 4.0 expectations (data-driven decisions, connectivity, security, and maturity). How you will contribute: Lead, coordinate, and develop technology visions, strategies, and execution roadmaps for D P equipment technologies to accelerate innovation programs and improve network performance. Provide inputs for and/or own parts of the innovation roadmap for process engineering strategies; ensure D P technology choices are benchmarked against peers and best-known methods. Actively scout technology and participate in industry conferences/forums to identify emerging solutions and translate them into deployable, value-based initiatives. Drive D P technology strategies that leverage digitalization for faster decision-making and improved control over operations, quality, and compliance - recognizing increased connectedness. Drive awareness of advanced manufacturing expectations and evolving global guidance as relevant to D P equipment strategies and future platform decisions. Lead D P process engineering contributions by defining technical strategies and providing critical D P manufacturing support across multiple sites (matrix). Lead evaluation of existing processes/equipment and define improvements to yield, efficiency, robustness and operability while maintaining acceptable quality. Establish/lead technology groups and Communities of Practice (CoPs) to harmonize engineering technologies across sites and ensure sharing and application of best practices and expertise . Own/author standards, guidelines, templates for D P process equipment technologies; drive consistent interpretation and application across the network. Establish sustained, collaborative communication with the process engineering community to understand site needs, installed standards, rationales, and local constraints. Develop & nurture core competencies of site SMEs to build enduring technical capability and knowledge continuity. Provide technical SME support to CAPEX investment projects, Design Engineering function, and investment applications, including support to feasibility studies, FEED, scope definition, value engineering, and vendor audits/selection - particularly for critical cGMP aspects and innovation. Lead evaluation of equipment design selection criteria supporting network strategy, capital investments, lifecycle management, and tech transfer - balancing efficiency, capacity, safety, sustainability, standards, and regulatory requirements. Liaise with key internal stakeholders involved in development and deployment of current and future solutions (Global Engineering, sites, leadership teams, and cross-functional partners). What you bring to Takeda: Technical , s cientific and /or e ngineering degree with 10 -15 years of technical experience in biopharmaceutical / pharmaceutical engineering or similar industry. P roven knowledge in Engineering t echnologies supporting product development and/or manufacturing , ideally in Drug Product manufacturing equipment (e.g., Formulation, Fill & Finish, Inspection, Packaging). Strong technical, interpersonal, communication and leadership skills. Recognized as an expert and leader in their specific field (e.g., leads industry forums or invited speaker at conferences). Strong knowledge of cGMP/GLP regulations, ICH, FDA CMC , ISPE and PDA Guidance Documents is preferred. Knowledge of industry 4.0 technology. English fluency (Written/Oral). Proven capability of acquiring knowledge and applying problem-solving methodologies. Empowering our people to shine At Takeda, we earn the trust of society and our customers through our values of Takeda-ism: Integrity, Fairness, Honesty, Perseverance. We incorporate these va