
Senior Analytical Expert
11 hours ago
Your main duties will involve:
- Designing and planning complex scientific experiments for drug development projects across multiple clinical phases.
- Providing expert guidance to laboratory team members.
- Developing, reviewing, and approving high-quality analytical documentation while ensuring compliance with relevant regulations.
- Contributing to the overall analytical strategy.
- Presenting scientific results internally and contributing to publications.
- Maintaining effective communication with internal and external stakeholders.
Key Responsibilities Include Designing Planning and Interpreting Scientific Experiments for Drug Substance and Drug Product Development. Providing Expert Guidance to Laboratory Team Members. Writing Reviewing and Approving Analytical Documentation in a Timely Manner Contributing to Scientific Exchange Groups Reporting and Presenting ScientificTechnical Results Internally contributing to Publications Presentations and Patents Managing Interactions and Contributing a High Level of Collaboration with Internal and External Stakeholders Adhering to Quality Metrics Compliance and Good Documentation Practices following ALCOA+ principles GLP OQM HSE ISEC.
Role Requirements PhD in analytical chemistry or equivalent and a minimum 6 years experience or M. Pharma/M. Sc with a minimum of 12 years experience in the pharmaceutical industry in analytical research and development Experience in driving analytical activities in NCE across various phases of drug development complex injectables parenteral oligonucleotides peptides and late phase method validation Good knowledge of software and computer tools such as Office package LIMS chromatography data-evaluation software e.g. Chromeleon Fluent English oral and written GMP experience in analytical laboratory Successfully demonstrated expertise in a specific scientifictechnical area Good presentation skills and scientifictechnical writing skills Good communication skills.
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