Scientific Associate - Analytical Development and Quality Control

• Gain the opportunity to work across several therapeutic areas including cardiovascular, immunology, and neuroscience.
• You will have the chance to work on several novel, innovative platform technologies.
• Experience for yourself what it’s like to work in a company that is internationally recognized as a 'top employer'.
• Enjoy being part of a collaborative work environment.

• Your primary responsibility will be the development, assessment, optimization, verification and conduct of analytical methods for a broad range of techniques such as purity-, stability-, content and potentially genotoxic impurity determinations.
• Conducting various analyses including release, retest, stability, transfer and validation.
• Protocol and report writing and documentation.
• Maintaining and operating analytical equipment.
• Planning and executing experiments, including forced degradation studies.
• Interpreting and documenting analytical data and activities.
• Drafting CoAs, Analytical results sheet, and SOPs.
• Training laboratory personnel and ensuring laboratory cleanliness.

• Graduate degree in analytical chemistry, pharmaceutical chemistry or related degree.
• Good knowledge of sample preparation, HPLC instrumentation and techniques, UV/VIS, IR.
• Demonstrable industry experience.
• GMP expertise.
• English (advanced).

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