Senior Manager, Bioreactor Process Development

Job Title: Senior Manager, Bioreactor Process DevelopmentLocation: ToulouseDepartment: Process and Product DesignReports To: Director of Process SciencesAbout Us: this is who we areAt Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated.Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCUREious with us and see where your curiosity can take youThe Role: Your challenge …in our journeyWe’re looking for a passionate and curious Senior Manager, Bioreactor Process Developmentto join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.As a Senior Manager, Bioreactor Process Developmentat Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.What You’ll Do:Leading a diverse group of scientists encompassing all aspects of cell culture and bioreactor process development, characterization, and validation as well as technology transfer to cGMP manufacturing for perfusion and intensified fed-batch processes.Collaborating across the organization to accelerate clinical development timelines, reduce development costs, and optimize strategies for process development and characterization for upstream bioreactor processes.Defining and driving the technology development strategy for process intensification and continuous manufacturing to reduce manufacturing costs and footprint through improvements in culture productivity, control of product quality, and data management while working with vendors and external partners.Serving as a Project Team Lead within the process development organization to execute on client projects that involve multiple functional areas and the full range of regulatory stages.Managing staff, training, capital resources, and planning within the department while supporting multiple client projects at various stages of process development and characterization.Serving as an internal technical resource for cGMP manufacturing and Process Design as well as a resource and subject matter expert for external clients and partners for cell culture and bioreactor processes (small scale models, process transfer, and scale up) in addition to authoring CMC regulatory sections.Clearly and effectively communicating scientific information, experimental plans, and data to internal project teams, cross-functional area teams, senior management, external clients, vendors, and technology development collaborators as well as the external scientific community such as regulatory agencies, review boards, publications, and conferences; may also be invited to present and lead scientific meetings, committees, and workstreams.Who You Are :Expert in bioreactor cell culture and perfusion technology development and tech as well ass CMC sections authoring for regulatory filings.Experienced in Biosimilar developmentExperienced with commercial process development, process characterization, and validation.Expert in design of experiments (DOE) and statistical analysis.Experienced with high throughput cell culture (e.g. HT assays, robotics such as Ambr systems, lab automation, or multi-omic data) is a plus.PlusesExperienced analyzing data in tools such as JMP, R, or Python.General understanding of cell biology, fluid dynamics, and biotransport as well as knowledge in other functional areas (downstream purification and analytical sciences).General understanding of circuits (grounding, power, signal, etc.).Experienced working in a cGMP or clean room setting (this job is non-GMP but knowledge of GMP is helpful for process/tech transfer activities).Master’s in engineering, Biochemistry, Biology, or related field with 12+ years of experience or Ph.D. in Engineering, Biochemistry, Biology, or related field with 10+ years of experience.Proficient in both verbal and written English is essential.Available to work on weekends and evenings is required.Why Join Us:Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life.Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.Are You Still Curious?If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Just Evotec Biologics.Let your curiosity guide your career—#BeCUREious and explore the endless possibilities at Just Evotec Biologics FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities. #J-18808-Ljbffr