Senior Process Engineering Manager

Job Title: Senior Process Engineering Manager Location: Toulouse Department: MSAT-MTS Reports To: Senior MTS manager 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. What You'll Do: Manage the process equipment team for upstream and downstream processes as well as for solution preparation. Strive to implement a continuous improvement mindset and standardization across the team and in alignment with stakeholders (Manufacturing, Quality, Global teams...). Implement Continuous Process Verification (CPV) and associated control plans. Be in charge of process control of manufacturing equipment ensuring production stability and performance level. Provide technical support and troubleshooting for critical manufacturing operations during engineering and GMP processing. Lead implementation of new technologies in production. Be in charge of manufacturing equipment maintenance plan definition and excellent execution in alignment with the maintenance planner. Support creation and review of technical documentation including batch records and reports related to engineering, GMP and PPQ runs. Support CQV activities by bringing expertise and leadership. Who You Are: Bachelor's degree in engineering science or a related program with 5+ years of relevant experience. At least 3+ years of experience managing technical teams in the bio‑pharma industry. Experience with equipment commissioning, qualification and validation activities. Operation in process control systems and development of automation recipes. Ability to organize, analyze/interpret, and effectively communicate data. Basic knowledge in statistics and more specifically with SPC. Familiar with continuous improvement approach and methodologies (e.g. RCA, DMAIC…). Authoring technical and quality documentation within GMP systems. Experience in process and equipment risk assessments using industry‑standard tools (e.g. FMEA). Experience with process analytical technology implementation and continued process verification. Understanding of chromatography, and filtration processing equipment and operations used to manufacture biotherapeutics. Good interpersonal, team, and collaborative skills are a must. Excellent oral and written communication skills in both English and French. Additional Preferred Qualifications: Applies knowledge to solve complex technical problems; may apply novel approaches that provide significant technology advancement. Ability to navigate global regulatory CMC documents. Why Sandoz? Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year 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. Our momentum and entrepreneurial spirit are powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible‑hybrid careers, where diversity is welcomed and where personal growth is encouraged 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. #J-18808-Ljbffr