MSAT Engineer (m/f/d) Downstream - 2 year contract

Job description

Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions – together with our clients. Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability. As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives. As an MSAT Engineer (m/f/d), you will support the project work in the Early, Late, and Commercial Stage phases in close collaboration with the Process Manager. Furthermore, you will have the chance to independently work on internal optimization projects. Your commitment and expertise will significantly contribute to the development and efficiency enhancement of our processes. Tasks and responsibilitiesPreparation of teleconferences and face-to-face meetings Documentation, evaluation, and verification of process and analytical data Creation, maintenance, and evaluation of trend tables Creation and review of GMP documents Support in handling deviations and change processes Participation/coordination/leadership of focus groups in the context of optimization projects Revision of concepts and SOPs What is important to usCompleted studies (Master) in Biotechnology, Bioprocess Engineering or comparable, or completed vocational training with additional further education and relevant professional experience In-depth knowledge of biotechnological development and production processes Strong communication skills, organizational talent, teamwork ability, economic and analytical thinking and acting Business fluent in German and English High level of initiative What you can look forward toMeaningful Work: Become part of a company that makes a real difference for critically ill patients by developing and producing vital medications Inspiring Work Atmosphere: Experience the joy of working in a collegial environment that promotes collaboration and team spirit on-site Individual Development Opportunities: Access to personalized training programs Compensation: Attractive salary and 13th-month salary Flexible Work Arrangements: Flexible working hours, options for remote work, 30 vacation days, and special leave days Communal Breaks: Cafeteria with vegetarian/vegan options Health: Corporate health management, company doctor, EGYM Wellpass Shared Experiences: Team and company events Employee Benefits: Variety of employee discounts (corporate benefits), discounts on the job ticket, financial relocation support beyond a certain distance, free parking, comprehensive onboarding program