Senior Bioprocess Engineer (m/w/d) 80%-100%

Senior Bioprocess Engineer (m/w/d) 80%-100% The actual location of this position is in Visp, Switzerland. Eligible applicants and their families are provided with relocation assistance as needed. As Senior Bioprocess Engineer - Senior Expert Biotechnologist Manufacturing, you will play a central role in the successful execution of GMP production campaigns and drive the technical advancement of biotechnological manufacturing processes. You will work closely with cross-functional teams, promote continuous improvements, and support the professional development of employees in a dynamic production environment. This position is a fully site-bound role. The close personal collaboration on site enables direct coordination in real-time and supports the technical precision required for the manufacture of medicines according to the highest quality and safety standards. What awaits you An agile career and a dynamic work culture. An integrative and ethical work environment. Compensation programs that recognize high performance. An expert role with high technical responsibility and visibility within the organization. The opportunity to actively shape production processes and technical strategies. Collaboration with multidisciplinary teams from Manufacturing, MSAT, Quality, and Engineering. You can find the full list of our global benefits here: https://www.lonza.com/careers/benefits Your tasks Responsibility for the GMP-compliant execution and technical support of production campaigns in the Upstream and Downstream areas. Creation, review, and implementation of risk analyses as well as tracking of resulting measures. Ensuring successful batch execution including data analysis, evaluation of test results, troubleshooting, and development of sustainable solutions. Ensuring complete and high-quality GMP documentation as well as documentation of process knowledge. Identification and implementation of improvement opportunities for processes, facilities, and workflows in close collaboration with MSAT and other stakeholders. Responsibility for product-specific campaign training as well as support for cross-functional training of employees. Promoting professional development within the team through coaching, workshops, presentations, and support during audits and inspections. What we are looking for Bachelor's or Master's degree in Biotechnology, Bioinformatics, Chemical Engineering, or a related natural science-technical field. At least 3 years of experience in pharmaceutical or biotechnological production with in-depth GMP understanding. Experience in the maintenance and optimization of biotechnological production processes, ideally in USP and/or DSP environments. In-depth knowledge of handling deviations, risk analyses, process improvements, and GMP documentation. Pronounced analytical skills as well as a structured and solution-oriented approach to work. Proven cross-functional leadership skills and potential for assuming direct leadership responsibility. Fluent German and English skills as well as excellent communication and training skills. About Lonza At Lonza, our employees are our greatest strength. At over 30 sites on five continents, our globally networked teams work together every day to manufacture the medicines of tomorrow. Our core values - collaboration, responsibility, excellence, passion, and integrity - reflect who we are and how we work together. The ideas of each individual, whether big or small, have the potential to improve millions of lives, and that's exactly what we want to share with you. Innovation thrives when people from diverse backgrounds bring their unique perspectives. At Lonza, we value diversity and strive for an integrative environment for all employees. If you are ready to turn our customers' groundbreaking ideas into practicable therapies, we look forward to welcoming you on board. Ready to shape the future of Life Sciences? Apply now!