pstrongBELIEVE IN LIFE. Join a company that takes you further! /strong /ppGalenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality affordable pharmaceuticals worldwide. /ppPeople are the key to our present and future success, so we carefully select candidates that meet the requirements for each position, however most importantly, who also fit with our cultural DNA and values. /ppstrongHere’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) /strong /ppWe are looking for a Stability Technician to join our Laboratory Team. /ppstrongWhat you'll be rocking: /strong /pulliRevision of stability reports issued RD projects done by RD (lab) and/or performed by externalised companies. /liliOrganize, manage and revise stability reports and results as part of Technical Transfers generated at 2n CMOs, including follow-up for Galenicum’s factory (SAG Manufacturer). /liliManagement and revision of on-going stability studies (products controlled or/and released by the lab, products manufactured in third CMOs or products where Galenicum is involved only as a broker). /liliEvaluation of trends and pourabilities on a regular basis in order to detect tendency and take preventive actions with CMOs. /liliRevision and approval of stability protocols, approval of stability protocols reports, follow-up of stability results at each time point, review of results and trends. /liliUp-to-date results in a common platform that can be consulted by each department.



/liliInform to inform all related departments of any expected deviation and coordinate new analysis if necessary. /liliCreate and maintain SOP related with these activities and train accordingly the staff. /li /ulpstrongWhat you bring to the table: /strong /pulliMinimum 1-2 years experience in analytical development in GLP/GMP environment, showing proven experience in the development and validation of most of the following analytical methods: HPLC, UPLC, LC-MS, GC, UV, DSC, PSD, potentiometric titration, UV-Vis, IR, AA, KF titrations and dissolution tests. /liliExperience in monitoring stability studies, analytical transfers from CRO’s to CMO’s and compiling technical documentation for obtaining MA internationally. /liliVery valuable to have knowledge of international guidelines EMEA, FDA, ICH and ISO. /liliExperience in MS Office. /li /ulpstrongEducational milestone: /strong /pulliDegree in life sciences, preferably in Pharmacy. /liliAdvanced level of English and Spanish, spoken and written. /li /ulpstrongYour key superpowers: /strong /pulliMotivated, proactive, dynamic, methodical, organized and decisive. /liliSelf-sufficient, influencing and leadership skills. /liliStrong analytical skills and problem solving. /liliHighly responsible and capable of working under pressure to meet deadlines. /liliAbility to prioritize multiple tasks /liliGood team player. /liliStrong organizational, planning and time management skills, to achieve project timelines. /liliDetail oriented and good communication and research skills. /li /ulpWe’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? /p #J-18808-Ljbffr

📌 Stability Technician (Barcelona)
🏢 Galenicum
📍 Barcelona