Technical Assistant – GMP Group (f/m/d)

Purpose of your Job

We are seeking a highly motivated and detail-oriented Technical Assistant to join our GMP Group at Coriolis Pharma. In this role, you will assist our scientific team by performing routine tasks under GMP regulations to support client projects and analytics as part of the commercialization process of their drug products. This position is ideal for individuals looking to gain hands-on experience in a regulated laboratory environment while working on a variety of client-driven projects within a dynamic, international and collaborative team.

Your Responsibility

• Support Client Projects: Assist scientists with the preparation and execution of routine analytical testing methods, such as chromatography, spectroscopy, and other standard assays for client projects under GMP regulations.
• Sample Handling: Support the preparation and handling of samples for testing, including labeling, storage, and tracking of materials used in client projects.
• Data Entry: Enter test results and other relevant data into project-specific databases or laboratory information management systems (LIMS) following appropriate protocols.
• Collaboration with Scientists: Work collaboratively and closely with project teams to support the efficient execution of client projects and provide any additional support required for project progression.
• GMP Compliance: Ensure all tasks are completed in strict adherence to GMP guidelines, following standard operating procedures (SOPs) and ensuring proper documentation of activities.
• Documentation and Reporting: Maintain accurate records of analytical processes, results, and materials used. Assist in the preparation of project documentation and analytical reports for clients.

What you need to succeed

• Technical training (e.g., CTA, PTA, MTA, or similar qualification).
• Ideally, 3-5 years of experience in a laboratory environment, preferably in a GMP-regulated setting. Experience in the biopharmaceutical industry is a plus.
• Basic understanding of GMP guidelines and regulatory requirements in the pharmaceutical industry.
• Ability to perform repetitive tasks with high attention to detail, ensuring accuracy in all steps of the analytical process.
• Strong organizational skills and the ability to manage multiple tasks and priorities efficiently.
• Basic knowledge of laboratory instruments and analytical techniques.
• Strong communication skills in English (German is a plus) and the ability to work effectively in a team environment.
• Proficient in Microsoft Office Suite; experience with laboratory information management systems (LIMS) is an advantage.

Your Contact

Dominik Schwemmer
Senior Business Partner - Talent & Development
People, Organization & Culture Unit

Coriolis Pharma Research GmbH
Phone: +49 (0) 89 – 417760 - 0
Fraunhoferstraße 18 b, 82152 Martinsried
www.coriolis-pharma.com