technical r&d senior associate scientist (m/w/d).

This position is within the field of analytical development for synthetic molecules, where state-of-the-art techniques such as high-performance liquid chromatography, gas/ion chromatography, and mass spectrometry are used to develop efficient and robust analytical methods. The goal is to ensure the release of products for clinical trials and their subsequent commercial supply through a rigorous control strategy.

General Information: 
 

• Start date: ASAP
• Duration: until 31.12.2026 with a possibility of extension
• Contract: contract of employment via Randstad
• Workplace: Basel 
• Workload: 100%
• Home Office: only occasional, mainly on-site
• Working hours: Standard

 

Tasks & Responsibilities:
 

• Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for quality assessment of starting materials, intermediates, and active pharmaceutical ingredients.
• 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 the smooth transfer of developed analytical methods.
• Creation of high-quality documentation, including analytical procedures and reports, which serve as the basis for method validations and regulatory submissions.
• Application of an innovative mindset and digital tools to continuously improve analytical workflows in a dynamic environment.

Must-Haves:
 

• Completed vocational training in a scientific field (laboratory technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 5 years of professional experience in the pharmaceutical industry (PhD graduates are considered overqualified)
• Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) and extensive knowledge of method development
• Excellent scientific writing skills and the ability to concisely summarize and present the results of complex experiments
• Strong quality awareness and uncompromising attention to detail, even when working in a non-GMP development environment
• Proactive, self-motivated work style and the ability to quickly adapt to new tools and processes in a dynamic team environment
• Fluent German and good written and spoken English skills

Nice-to-haves:
 

• Knowledge of GxP requirements and method validation is advantageous

Take a leading role in the development of innovative analytical techniques and contribute to the success of clinical and commercial therapies – apply now and help shape the future of healthcare!