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Employee (m/f/d) for organic chemistry in the Manufacturing Science and Technology department
vor 2 Monaten
Enter the world of innovation and cutting-edge research in a leading international company.
Our dynamic team in the heart of picturesque Penzberg sets new standards in the development of groundbreaking medical solutions. We offer ambitious talents the opportunity to contribute and further develop their expertise as an employee (m/f/d) for organic chemistry in the Manufacturing Science and Technology department.
Here's what we offer
Completed training as a technician in chemistry, biotechnology or similar or a degree with a technical or scientific focus (e.g. biotechnology or similar) Sound professional experience in the field of production or quality assurance in a GMP environment (*not* career starters) Strong quality management background Fluent German and (at least) good English skills IT affinity and ability to quickly familiarize yourself with new tools Ability to adapt to different stakeholders
Your tasks
Technical initiation and planning of troubleshooting, efficiency and quality assurance projects Implementation, adaptation and testing of production processes Establishment of new synthesis and purification processes Collaboration/management of higher-level troubleshooting Provision of technical expertise in the creation of regulations Support in the production of transfer approaches and documentation in accordance with GMP guidelines Compliance with safety and regulatory guidelines (FDA, USDA, QM system) Coordination and leadership to ensure the achievement of project goals (quality, deadline, costs) Collaboration in resource management and efficiency improvement measures Comprehensive stakeholder information
Your profile
Adoption of new production processes/products from RnD Initiation, planning and implementation of troubleshooting, efficiency and QA projects Management/cooperation in troubleshooting projects Establishment of new synthesis and purification processes Adaptation and testing of production processes Technical support in the preparation of regulations and GMP-compliant documentation Compliance with safety guidelines Management/coordination of target achievement (quality, deadlines, costs) Resource management for optimal production processes Compliance with QM and regulatory requirements (e.g. FDA, USDA) Information for stakeholders Practical experience in a GxP-regulated environment desirable