Lab Associate - Oligonucleotides Analytics; m​/w​/d

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

The position is located in Analytical Research and Development for Synthetic molecules within Pharma Technical Development. The team 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:

• Duration: 12 months
• Extension: possible
• Contract type: temporary contract via Randstad (employment)
• Work Location: Basel
• Home Office: up to 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 Open Lab 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.

Must Haves:

• Vocational scientific qualification as chemical laboratory technician (e.g. apprenticeship) with at least 2-3 years experience in the pharmaceutical industry (MSc and PhD 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.