> Markdown version of [/jobs/ext/4060236-scientist-lc-gc](https://www.wearedevelopers.com/jobs/ext/4060236-scientist-lc-gc). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Scientist LC & GC - **Company:** Amaris - **Location:** Beerse, Belgium (Remote available) - **Contract:** Permanent contract - **Skills:** Data Integrity, Data Systems - **Published:** October 26, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=7910d9a68d742e12 ## About the Role * Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific field, or a Bachelor's degree with relevant laboratory experience. * Strong hands-on experience in liquid chromatography (LC), ion chromatography (IC), and/or gas chromatography (GC), including headspace and liquid injection for GC. * Experience in analytical method development and validation is required. * Experience with chromatography data systems (CDS), preferably Empower and/or OpenLab. * General knowledge of cGMP requirements and experience working in a regulated laboratory environment. * Experience with, or willingness to develop expertise in, other analytical characterization techniques such as water determination and titrations. * High standards for experimental quality, data reliability, and accountability for results. * Ability to work independently, manage priorities effectively, adapt to changing needs, and collaborate with cross-functional teams. * Fluent in written and spoken English. ## Description * Perform analyses for Reference Standard characterization, with a focus on liquid chromatography (LC), ion chromatography (IC), and gas chromatography (GC), including headspace and liquid injection. * Develop fit-for-purpose LC, IC, and/or GC methods to support accurate purity determination at low reporting thresholds. * Support product and process characterization, method development, validation, release, and stability activities. * Evaluate analytical results, draw relevant conclusions, and communicate findings to project stakeholders. * Use chromatography data systems (CDS), such as Empower and/or OpenLab, to generate and document reliable data. * Ensure compliance with GMP requirements, safety standards, analytical methods, specifications, and applicable regulatory guidelines. * Manage priorities effectively, take ownership of experimental work, and contribute independently and collaboratively to project activities.