Technical R&D Associate Scientist
vor 2 Wochen
Location:
Basel, Switzerland
Duration:
12 months (extension possible)
Workload:
100%
On-site:
approx. 90% (max. 10% remote)
About the Role
You will join a global technical development organization dedicated to advancing innovative medicines through cutting-edge science, collaboration, and high-quality execution. Within the Analytical Research & Development group for synthetic molecules, you will help develop and refine robust analytical approaches that support both clinical development and future commercial supply.
The team focuses on creating cost-efficient, reliable analytical methods using state-of-the-art techniques such as HPLC, MS, LC-MS, gas chromatography, and ion chromatography. Your contribution will support essential control strategies and ensure the delivery of high-quality products for clinical studies.
Key Responsibilities
- Develop, improve, and validate analytical methods for starting materials, intermediates, reaction monitoring, active substances, and galenical forms
- Plan, execute, and document laboratory experiments according to GxP guidelines and internal SOPs
- Collaborate with scientists, associate scientists, and cross-functional partners to support efficient end-to-end analytical workflows
- Coordinate analytical activities, including sample management for synthetic molecule development
- Prepare scientific documentation such as analytical procedures, validation reports, user manuals, and SOPs
Your Profile
- Completed vocational scientific qualification with
3-5 years of experience
in pharmaceutical analytical development for oligonucleotides
OR
Bachelor/Master's degree in Analytical Chemistry, Biochemistry, Biotechnology or related field - Solid hands-on experience with
HPLC
and
MS
instrumentation - Knowledge of
LC-MS
applications (strong advantage) - Strong interest in or background with oligonucleotide analytics
- Excellent digital skills and openness to innovative tools and agile ways of working
- Detail-oriented, quality-driven mindset and strong documentation skills
- Self-motivated, proactive, reliable, and an excellent team player
- Fluent in
English
; German skills are an advantage - Sound understanding of GxP requirements across multiple clinical phases
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