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Scientist Method Development Chromatography
Job description
As a Scientist at Anabiotec, you will act as a scientific lead in the analytical lifecycle of (bio)-pharmaceutical products. Your mission is to bridge the gap between complex client needs and robust laboratory solutions.
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Design, optimize, and troubleshoot complex chromatographic methods (primarily HPLC/UPLC) for a diverse portfolio, including small molecules, peptides, oligonucleotides, and proteins/antibodies.
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You will act as the Subject Matter Expert (SME) for Liquid Chromatography guiding the lab team through technical hurdles.
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Interact with international biopharma clients to define analytical strategies, discuss scientific data, and provide expert advice on regulatory requirements.
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You lead the transition of methods from development to qualification and validation, ensuring they are "fit-for-purpose" according to ICH guidelines.
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Uphold the highest standards of data integrity. Ensure all work is documented and reported according to Good Documentation Practices (GDocP) and within the framework of GLP/GMP environments where required.
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Innovation & Efficiency: Implement Design of Experiments (DoE) and Quality by Design (QbD) principles to streamline development and ensure method robustness.
Profile
We are looking for a scientist who combines deep technical hands-on expertise with the strategic mindset required to thrive in a fast-paced CRO.
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PhD in Chemistry, Pharmacy, Biochemistry, or a related scientific field. Candidates with a Master’s degree and extensive, high-level industry experience in method development are also encouraged to apply.
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Technical Expertise
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Expert-level knowledge of LC (HPLC/UPLC) and Mass Spectrometry (LC-MS/MS).
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Proven experience working with "New Modalities": Oligonucleotides (IP-RP, AEX), Peptides, and Large Molecules (mAbs, proteins) is a plus.
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Experience with Empower and Chromeleon
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Familiarity with other separation techniques like Gas Chromatography (GC) and Capillary Electrophoresis (CE) is an advantage.
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Understanding of ICH Q14 principles and method validation according to ICH Q2 within GxP environments and a commitment to meticulous documentation.
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Knowledge of statistical tools and Design of Experiments (DoE) is a plus.
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You have the ability to look beyond the immediate test and understand the client's broader drug development goals.
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Comfortable managing multiple projects simultaneously in a dynamic, deadline-driven laboratory environment.
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Excellent command of English (written and spoken). Ability to translate complex data into clear reports and presentations for clients. Knowledge of Dutch is an asset.
Offer
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You will be part of the anacura group, a family owned, long term focused and ambitious laboratory organization.
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You will join a dynamic team and have a position with autonomy and responsibility with opportunities to take initiatives to support further growth.
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You will be offered a competitive salary with fringe benefits, a green work environment and the possibility to join our bike lease program, flexible working hours, a healthy lunch, and a pleasant fun club.
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You are stimulated in your personal growth; we build on your talents in accordance with our ambitions.
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