Ph3Overview /h3 ul liLocation: Ancona (Italy) /li liContract: Temporary /li liWorking day: Tempo pieno /li liSector: Pharmaceutical and biopharmaceutical /li liVacancies: 1 /li liDiscipline: Quality /li liWork modality: On site /li /ul pKymos Group – 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. We offer GMP/GLP‑certified and GCP‑compliant services, spanning small and large molecules, generics, biosimilars, antibodies, biomarkers, ADA, ADC, hormones, enzymes, and nucleic acids. /p pbScientist – Quality Control /b /p h3Responsibilities /h3 ul liThe design, supervision, and execution of quality control studies. /li liManaging the assigned projects, keeping deadlines and maintaining direct contact with the client. /li liTechnical document writing associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.). /li liDirecting and supervising the experimental work of the technical staff in charge. /li /ul pWe offer a position in a growing company with international projection and a salary based on experience and knowledge. /p h3Requirements /h3 ul liDegree/Laurea in Chemistry, Pharmacy or equivalent. /li liMinimum 2 years of experience in chemical analysis of active principles and pharmaceutical forms in Analytical Development and Quality Control departments in the pharmaceutical sector. /li liProficiency in HPLC/UHPLC, CG, and basic analytical development techniques such as dissolution tests, potentiometry, Karl Fischer, atomic absorption, etc. /li liHigh level of English. /li /ul pKymos considers diversity and inclusion as key development priorities, with a main goal of promoting a culture that embraces differences and celebrates unique talents. We are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic. /p /p #J-18808-Ljbffr