Senior Manager, Bioreactor Process Development (all genders)

Responsibilities

• 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.
• 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.

Requirements

• Expert in bioreactor cell culture and perfusion technology development and tech as well as CMC sections authoring for regulatory filings.
• Experienced in Biosimilar development
• Experienced 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.
• Pluses
• Experienced 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 Sandoz?
• Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz , a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
• With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
• The future is ours to shape!
• 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.

Benefits

Additional Information

Job Title: Senior Manager, Bioreactor Process Development Location: Toulouse Department: Process and Product Design Reports To: Director of Process Sciences We're excited to share this opportunity is part of the Sandoz acquisition of Just-Evotec Biologics in Toulouse. Through this opportunity you will impact the lives of hundreds of millions of people through bold ideas supported by an inclusive, agile company culture. Join us to help make healthcare fairer and faster, help us to pioneer access to medicine! Click to learn more.

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