Pharmaprogress is a reliable Contract Research Organization part of the Kymos Group, a fast-growing company with a strong commitment to quality and a dedication to innovation. Our customers have access to a wide range of GMP / GLP-certified and GCP-compliant services and obtain a tailor-made, personalized, genuinely flexible service into a unique selection of services for innovative small and large molecules, generics, biosimilars, antibodies, biomarkers, ADA (anti-drug antibodies), ADC (antibody-drug conjugates), hormones, enzymes, and nucleic acids. We are looking for an Analyst in testing and certification of raw materials to ensure the correct development of assigned analytical projects. The responsibilities of the position include : Developing samples and using analytical techniques to determine physical / chemical properties. Performing the work in compliance with Good Laboratory Practices and GMP. Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion, or any other personal characteristic. Requirements Higher education in Laboratory Analysis and Quality Control. Experience working with HPLC and GC. Experience in GMP environments is an asset. Skilled in physical / chemical properties determination. Familiar with the use of Pharmacopoeias. 1 year of experience in similar roles in the pharmaceutical industry. Sector : Pharmaceutical and biopharmaceutical J-18808-Ljbffr J-18808-Ljbffr