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Analytical Development Expert

vor 7 Monaten


Aachen, Deutschland Grünenthal Vollzeit

**Country**:Germany**City**:Aachen**Department**:Global Operations & Production**Job ID**:44115- Our people in **Manufacturing & Global Operations** share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit in well here. It’s an international team with a powerful spirit of collaboration. Together, we make sure our products meet the highest standards of quality by constantly searching for ways to improve at every stage of our value chain - from the raw materials we buy through to the logistics network that brings our medicines to patients. Join our team and help us make an even bigger contribution to Grünenthal’s future.**What the job looks like**
Each day you’ll enjoy a variety of challenges, such as:
- Supervision and coordination of analytical development projects;coordination of internal and external project activities for release of APIs and pharmaceutical formulations
- Monitoring, review and evaluation of project-related documents according to GMP-guidelines
- Development and continuous optimisation of analytical methods in collaboration with the laboratory's technical staff
- Coordination of external CDMOs
- Scientific and technical support for the LATAM commercial product portfolio
- Scientific management of projects for the clarification, quantification of genotoxic impurities and establishment of the required analytical methods, in-house or in cooperation with specialised external laboratories, for the Grünenthal portfolio
- Transfer of analytical methods
- Creation and review of standard operating procedures (SOP)
- Initiating the implementation and approval of specifications in the LIMS

**What you’ll bring to the table**
To make the most of this role and truly thrive, you should have:
- Successfully completed studies as a chemist or pharmacist or equivalent
- Professional experience in analytical drug development (analytical method development, validation, troubleshooting)
- Hands on experience in GMP regulated environment
- Proven expertise in instrumental analysis
- Fluent written and spoken English, German is a plus