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! 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).
Quality & Regulatory Compliance :
Manage deviations, CAPAs, change controls, and out-of-specification (OOS) results in compliance with regulatory guidelines.
Business Development, Finance, Technical Support) to ensure seamless project execution.
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.
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, or CAD detection
Professional experience in a GMP-controlled environment with in-depth understanding of GMP regulations, quality management systems, and compliance standards
Demonstrated project management experience with strong skills in resource management, multitasking, prioritization, and risk management
Hands-on, proactive mindset with openness to new ideas and tasks; Excellent verbal and written communication skills in English
Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, citizenship or gender identity, color, disability, religion/belief, sexual orientation, marital status, age or individual preferences. Different backgrounds, experiences and ideas push us further and raise the bar.
We would like to support you from the very beginning to shape your development possibilities here at Coriolis.
Coriolis Pharma Research GmbH
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. An additional project management and business development team in the United States enables our US clients to work seamlessly with our German offices.
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