Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d) in Basel

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a dedicated Analytical Associate.

This position is located within the Analytical Development for Synthetic Molecules department, where cutting-edge techniques such as High-Performance Liquid Chromatography (HPLC), Gas/Ion Chromatography (GC/IC), and Mass Spectrometry (MS) are used to develop efficient and robust analytical methods. The goal is to ensure product release for clinical trials and subsequent commercial supply through a rigorous control strategy.

General Information:

• Duration: 1 year
• Extension: likely
• Contract type: Temporary contract via Randstad (employment)
• Work Location: Basel
• Home Office: not possible
• Working Hours: Standard

Tasks & Responsibilities:

• Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (APIs).
• Planning and meticulous execution of experiments, including reaction monitoring and method development.
• Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management.
• Close cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods.
• Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings.
• Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment.

Must Haves:

• Completed vocational training in natural sciences (Laboratory Technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 2-3 years of professional experience in the pharmaceutical industry.
• Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development.
• Strong scientific writing skills and the ability to summarize and present results of complex experiments precisely.
• High quality awareness and uncompromising attention to detail, including work within a non-GMP development environment.
• Proactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment.
• Fluent English language skills (both spoken and written)

Nice to Have:

• Knowledge of GxP requirements and method validation

Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies

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