Associate Oligonucleotides Analytics (m/w/d)

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for an Associate Oligonucleotides Analytics.

About the job: 

Analytical Development for synthetic molecules is responsible for the development of resource and cost-efficient analytical methods by use of state of the art and innovative techniques such as high-performance liquid chromatography, gas or ion chromatography or mass spectrometry. The ultimate goal of our work is the development of a robust control strategy to release products for clinical trials, and finally for commercial supply.

General Information: 
 

• Start date: May 2026
• Duration: 1 year
• Contract: temporary contract via Randstad
• Extension: possible
• Workplace: Basel 
• Workload: 100%
• Home Office: max. 10%
• Working hours: Standard

Tasks & Responsibilities:
 

• Performing routine measurements for Oligonucleotides (mainly HPLC with UV and/or Single Quad MS detection)
• Planning, executing, and documenting experiments collaboratively in a team of five associates.
• Use chromatographic data systems like Empower or OpenLab to control analytical instruments.
• Evaluate data with Genedata or Oligo Analysis Accelerator
• Developing, improving, and validating analytical methods for the quality assessment of Oligonucleotides.
• Ensuring compliance with GxP guidelines and relevant SOPs.

• Vocational scientific qualification as chemical laboratory technician (e.g. apprenticeship) with at least 2-3 years experience in the pharmaceutical industry (MSc graduates are considered overqualified)
• Hands-on experience with analytical instrumentation and techniques (e.g., HPLC, MS)
• Interest or background in analytical development for oligonucleotides
• Strong knowledge of LC-MS applications and instruments is a plus
• Experience with large molecules/biologics analytics is an advantage
• Self-motivated, proactive, open-minded, goal-oriented, and a strong team player
• Stringent quality mindset, excellent attention to detail, and knowledge of GxP requirements across clinical phases.
• Good command of English; German proficiency is beneficial.