Associate Scientist

Il y a 1 jour

Beerse, Flanders, Belgique DPS Group Global Temps plein
Analytical Development plays a critical role within a pharmaceutical R&D environment, providing end-to-end analytical support for synthetic drug substances and drug products throughout development. Within the Analytical Method and Stability Center (AMSC), the team supports both small molecules and new modalities, ensuring the successful progression of innovative therapeutics from clinical Phase 1 through registration. Your Role As an Associate Scientist, you will provide analytical support for new molecular entities, including small molecules and new modalities such as therapeutic peptides, conjugates and oligonucleotides. You will support analytical activities across the development portfolio for both drug substances and drug products, with a strong focus on method development, validation and analytical testing.

Key Responsibilities
• Perform analytical testing in support of product and process characterization, method development, validation, release and stability studies.
• Work primarily with liquid chromatography (LC) and physico-chemical characterization techniques.
• Develop fit-for-purpose LC and/or physico-chemical methods, such as Karl Fischer and titration, meeting the required Low-Level Reporting Threshold.
• Ensure compliance with relevant regulatory guidelines, analytical methods and specifications, GMP requirements and safety standards.
• Scientifically evaluate and interpret generated analytical results.
• Maintain high-quality standards and take ownership of experiments and results.

Your Profile
• You hold a Master’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry or a related scientific field, or a Bachelor’s degree with at least 3 years of relevant industrial experience.
• You have strong knowledge of and hands-on experience with liquid chromatography (LC) and/or physico-chemical techniques such as Karl Fischer and titration.
• You have knowledge of chromatography data systems (CDS), preferably Empower and/or OpenLab.
• Knowledge of physico-chemical analysis software such as Tiamo and/or Omnis is an advantage.
• Knowledge of cGMP regulations and practical GMP experience are considered a plus.
• You work accurately and take accountability for your experiments and results.
• You are efficient, flexible and able to adapt to changing priorities.
• You are customer-focused and results-driven.
• You can work independently while also being a collaborative team player with a positive can-do attitude.
• You are proficient in English, both spoken and written.