Analytical Scientist
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Scientist – Analytical Method & Stability Center (AMSC)
Want to make an application Make sure your CV is up to date, then read the following job specs carefully before applying.
Beerse, Belgium | Contract | ASAP start – until 31/12/2026 (with likely extension into 2027)
Are you a driven analytical scientist ready to make an impact in pharmaceutical R&D? We're recruiting on behalf of a leading global pharmaceutical innovator for a Scientist to join their Analytical Method & Stability Center (AMSC), part of a broader Analytical Development organisation supporting synthetically designed drugs across the full product lifecycle.
About the role
You'll represent AMSC on cross-functional project teams, translating project needs into laboratory activities that support analytical method development, product characterization, stability profiling, and clinical release testing. You'll work on assigned R&D programs spanning synthetic modalities including oligonucleotides, peptides, conjugates, and degraders - collaborating closely with API and Drug Product development teams.
What you'll do
- Independently manage multiple assigned synthetic development projects, setting priorities aligned with project and team objectives
- Collaborate cross-functionally with other Analytical Development teams
- Drive product development through fit-for-purpose stability studies and characterization techniques, backed by strong scientific data interpretation
- Act as the technical link between drug substance/development teams and the analytical team
What you bring
- PhD in Analytical Chemistry, Pharmaceutical Technology or related field (0-3 years' experience), OR a Master's in Chemistry/Biochemistry with 3+ years' relevant experience
- Knowledge of stability studies (ICH stability, RIBPS, open dish stress studies)
- Experience developing, validating xlxgzvr and transferring analytical methods, ideally with a strong focus on Liquid Chromatography (LC/GC experience a strong plus)
- Familiarity with synthetics (conjugates, oligonucleotides, degraders) and their associated analytical/characterization techniques
- GMP knowledge and industry experience is an asset
- Strong project management instincts, a proactive attitude, and excellent communication skills
- Fluent English (spoken and written)
Details
- Fulltime onsite, with flexibility for WFH aligned with your manager
- Belgium-based candidates only
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