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Jobdescription
For our client, an international pharma company in Basel, we are looking for a motivated Technical R&D Senior Associate Scientist 

In this role you will be working in Analytical Development Synthetic Molecules within Pharma Technical Development which is responsible for the development of resource and cost efficient analytical methods using state of the art methodologies such as e.g. High-performance liquid chromatography (HPLC), Gas Chromatography (GC), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate goal of our work is a robust control strategy to release products for clinical trials, and finally for commercial supply.

General Information:

* Start date: ASAP
* Latest Start Date: October 2024
* Planned duration: 12 months
* Extension: possible
* Workplace: Basel
* Workload: 100%
* Remote/Home Office: max. 10% remote
* Team: 10 colleagues
* Working hours: Standard

Tasks & 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

Must Haves:

• Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, MS)
• Strong knowledge on LC-MS applications and instruments is a plus
• A strong interest/background in analytical development for peptides
• Experience in the field of large molecules/biologics analytics would be a plus
• 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

Marta Bartkowiak