Responsibilities:
Development, improvement and validation of analytical methods for the quality assessment of starting materials, intermediates, reaction monitoring, active substances and galenical forms.
Thorough and efficient planning, execution and documentation of experiments in collaboration with the relevant team members, analytical project lead and your supervisor, following current GxP guidelines as well as relevant SOPs.
Work on end-to-end processes in close collaboration with other associate scientists, scientists, and partners from other departments to ensure efficient analytics and continuous improvement.
Coordination of analytical activities, including sample management for the development of synthetic products.
Authoring of documents, e.g., analytical procedures, validation reports, user manuals, SOPs.
Minimum Requirements:
Apprenticeship or a Bachelor/Master in analytical chemistry or in a related field.
Work experience in a lab environment, preferably in the pharmaceutical industry.
Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, MS).
A good scientific writing style and good documentation practice for utilization of corresponding data in regulatory filings.
Excellent digital skills and an innovative mindset.
Preparedness to learn, continuously improve and apply novel ideas, tools and processes to quickly adapt to a fast-changing environment.
Self-motivated, open-minded, proactive, reliable, goal-oriented and an excellent team player.
You are open to new ways of working and support our team on the way to more flexibility and agility.
Excellent command of the English language. Good command of the German language would be a plus.
A stringent quality mindset and excellent attention to detail.
Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases.
Additional Information:
You will work in an international environment.
A very renowned company.
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