About this role

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.

Take a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies — apply now and help shape the future of healthcare

General Information:

Start date: November-December 2026
Duration: 1 year
Extension: likely
Contract type: Temporary contract via Randstad (employment)
Work Location: Basel
Workload: 100%
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: