Scientist Analytical Method
Il y a 11 heures
Antwerp, Flanders, Belgique
Pauwels Consulting
Temps plein
Gratuit avec email ou Google
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Gratuit avec email ou Google
Our client, a leading pharmaceutical organization, is seeking a Scientist to join their analytical development department. The role focuses on supporting stability assessment and method development for synthetic drug products across the full product lifecycle.
Support multiple assigned projects in synthetic development including oligonucleotides, peptides, and conjugates.
Collaborate with cross-functional teams across API and drug product development to align project objectives.
Initiate fit-for-purpose stability studies and characterization techniques to ensure product quality.
Perform deep scientific data interpretation to drive product development and characterization.
Oversee project timelines and priorities as a stability lead within the project team.
Translate laboratory results and protocols into actionable insights for diverse technical stakeholders.
You hold a PhD in Analytical Chemistry or Pharmaceutical Technology with 1+ years of experience, or a Master's degree with 3+ years of relevant experience.
You have experience with stability studies including ICH stability, RIBPS, and open dish stress studies.
You possess knowledge of drug substance synthesis and drug formulation processes for synthetics, conjugates, and oligonucleotides.
You bring a proactive attitude and strong project management skills to ensure results-driven outcomes.
You are fluent in English.
Nice to HavesExperience with Liquid Chromatography and Gas Chromatography analytical techniques.
Practical experience in an industrial setting and knowledge of GMP regulations.
Support multiple assigned projects in synthetic development including oligonucleotides, peptides, and conjugates.
Collaborate with cross-functional teams across API and drug product development to align project objectives.
Initiate fit-for-purpose stability studies and characterization techniques to ensure product quality.
Perform deep scientific data interpretation to drive product development and characterization.
Oversee project timelines and priorities as a stability lead within the project team.
Translate laboratory results and protocols into actionable insights for diverse technical stakeholders.
You hold a PhD in Analytical Chemistry or Pharmaceutical Technology with 1+ years of experience, or a Master's degree with 3+ years of relevant experience.
You have experience with stability studies including ICH stability, RIBPS, and open dish stress studies.
You possess knowledge of drug substance synthesis and drug formulation processes for synthetics, conjugates, and oligonucleotides.
You bring a proactive attitude and strong project management skills to ensure results-driven outcomes.
You are fluent in English.
Nice to HavesExperience with Liquid Chromatography and Gas Chromatography analytical techniques.
Practical experience in an industrial setting and knowledge of GMP regulations.