Coriolis Pharma is a global contract research and development organization (CRDO) and a premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a vast array of therapeutic modalities, including biologics, gene and cell therapies and vaccines.


Our scientists design and execute platform and custom services to accelerate and derisk our clients’ programs right from the start and throughout the entire product lifecycle.

Our company culture is based on diversity, teamwork and open and appreciative communication. That's why wonderful people from over 36 nations around the world work together successfully at Coriolis.
Our headquarters are located in Martinsried near Munich, Germany. An additional project management and business development team in the United States enables our US clients to work seamlessly with our German offices.

What motivates us? Our motivation is to improve the quality of life for humankind by enabling the development of innovative drugs through outstanding biopharmaceutical services from preclinical to commercialization As a Senior Scientist in GMP Analytical Services at Coriolis Pharma, you will leverage your scientific expertise to successfully guide complex customer projects within a GMP-regulated environment, ensuring that scientific objectives are met within quality and regulatory frameworks.
In this role, you will contribute to our state-of-the-art analytical services, applying advanced technologies to support the research and development of biopharmaceuticals and innovative drugs. You will be an integral part of our contract research organization-collaborating closely with and learning from our scientific operations teams-to enable our clients on their journey of developing cutting-edge therapeutics.

Join Coriolis Pharma - a science-driven service provider shaping the future of biopharmaceutical innovation!


Your Responsibility
Project Ownership & Scientific Expertise:


Responsible-together with the project team-for the successful development and execution of analytical services for our customers worldwide.
Act as subject matter expert, supporting client project acquisition and execution with your expertise to ensure high-quality services.
Lead analytical strategy and actively contribute to experimental execution in alignment with SOPs, pharmacopoeias, and project-specific requirements.
Apply laboratory techniques such as HPLC, particle analytics, and dynamic light scattering (DLS).
Integrate scientific knowledge and a deep understanding of regulatory standards to address evolving business needs, including new areas and novel molecular modalities.

Quality & Regulatory Compliance:


Ensure full adherence to QA and QC processes across all analytical activities.
Manage deviations, CAPAs, change controls, and out-of-specification (OOS) results in compliance with regulatory guidelines.

Collaboration & Process Excellence:


Collaborate closely with Coriolis teams (e.g., Business Development, Finance, Technical Support) to ensure seamless project execution.
Contribute to cross-functional initiatives, driving both scientific and operational improvements.
Support preparation of validation protocols, reports, and testing procedures.

Project Leadership & Knowledge Transfer:


Serve as project leader for client projects, overseeing planning, method implementation, development, characterization, data evaluation, and reporting.
Share your expertise with Coriolis team members and represent Coriolis’ scientific excellence within the broader scientific community.

University degree in analytical chemistry, pharmaceutical sciences, (bio)chemistry, or a related field; a PhD related to (U)HPLC method development or surfactant quantification is preferred
Minimum 5 years of industry experience (with PhD in a relevant field) or 9 years (without PhD) in biopharmaceutical characterization by LC (RP, SEC, IEX) using UV, FLD, RI, ...