Senior Scientist

**Purpose of your Job**:
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.

**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.
- Lead analytical strategy and actively contribute to experimental execution in alignment with SOPs, pharmacopoeias, and project-specific requirements.
- 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.

**What you need to succeed**:

- 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

- Proven expertise in GMP analytical method development, validation, characterization, and technology transfer for drug product development of biopharmaceuticals

- 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; lead by example with a can-do attitude

- Team-oriented with strong motivational and interpersonal skills

- Excellent verbal and written communication skills in English

**Why to join Coriolis?**:
**_ Let’s formulate innovation together _**:
**_We would like to grow together with you_**:

- Let’s continue building and creating the future now Join our Team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience. We offer an attractive work space at the Martinsried site. Let’s make a difference together_

**_Please use our career portal exclusively for this purpose._**:

- We would like to support you from the very beginning to shape your development possibilities here at Coriolis._
- For questions or further information, please visit our website or contact us directly._

**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_

**About us**:
**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 developm