Analytical Scientist

Panda International; Gierle; Sur place; EUR 52 000 - 78 000; Plein temps

Résumé du poste

Panda International seeks a Scientist for the Analytical Method & Stability Center (AMSC) in Beerse, Belgium. The role focuses on analytical method development, stability profiling, and clinical release testing within cross-functional teams.

Ideal candidates hold a PhD in Analytical Chemistry or related field (0–3 years) or a Master’s with 3+ years of relevant experience. Strong LC/GC skills and GMP exposure are preferred, with fluent English required.

Qualifications

• PhD or MSc with experience in analytical chemistry and GMP is preferred.
• Experience in stability studies (ICH stability) and product characterization.
• Experience developing, validating, and transferring analytical methods (LC/GC a plus).
• Familiarity with synthetic modalities (oligonucleotides, peptides, conjugates, degraders) and analytical techniques.

Responsabilités

• Independently manage multiple synthetic development projects with priorities aligned to goals.
• Collaborate cross-functionally with Analytical Development teams.
• Drive stability studies and product characterization to support development.
• Serve as technical link between drug substance teams and analytics group.

Connaissances

Project management

Communication skills

GMP knowledge

English language

Formation

PhD in Analytical Chemistry, Pharmaceutical Technology or related field

Master's in Chemistry/Biochemistry with 3+ years of experience

Outils

LC/GC

Description du poste

Scientist – Analytical Method & Stability Center (AMSC)

? 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 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