PpApply for the bQuality Control Raw Materials Analyst /b role at bBoehringer Ingelheim /b. /p h3The Position /h3 pWe are looking for a Quality Control Analyst for our Raw Materials Team, to support the increased analytical activities related to the introduction of a New Chemical Entity and to ensure compliance standards required by corporate and international authorities. /p h3Tasks Responsibilities /h3 ul liReports directly to the Raw Materials Coordinator /li liIndependently performs analytical testing required for the release of raw materials used in the synthesis of finished and semi‑finished products and in the in‑process controls /li liEnsures the correct procedures are adhered to, in terms of Quality, Environment Safety /li liRaises and investigates deviations and out of specifications within the QC department /li liPromotes, develops, and strives for continuous process improvements within the QC department including method development and evolving existing processes /li liWrites Protocols, Reports and Procedures (SOPs); learns the management system of the Quality Learning tools and procedures applied within the site /li liExecutes all assigned activities in compliance with established analytical procedures /li liCollaborates with the intermediate product release team when needed /li /ul h3Requirements /h3 ul liEducational background in chemistry or related fields /li li1-5 years of experience in the chemical‑pharmaceutical quality control field is preferred /li liGood knowledge of the main equipment used in quality control laboratories, particularly gas chromatographs (direct injection and Head‑Space), HPLC, potentiometric titrators, spectrophotometers, and atomic absorption/ICP‑MS /li liKnowledge of analytical discrepancy management workflows (OOX / Event / Deviations) and regulatory requirements in the pharmaceutical industry (GMP / ISO) /li liFamiliarity with laboratory data management software /li liGood understanding of written English /li liWillingness to work in shifts, including occasionally Saturdays and Sundays /li liTeamwork attitude /li /ul h3What we offer /h3 ul liA temporary contract with an external agency (24 months – Somministrazione) /li liFree access to the company canteen and ticket restaurants when working remotely. /li liA range of benefits for physical, financial, social and mental wellbeing (access to gyms, psychologist, volunteering, parental support, company welfare and more). /li liA support to develop your own professional and personal path that will guide you through our full range of development programs including platforms to learn foreign languages and attend professional courses. /li /ul h3Equal Opportunity Statement /h3 pWe are committed to guarantee equal opportunities; we believe in respect, trust and empathy, in a work environment without discrimination. We are powered by our people as we know that our differences are our strengths. We value everyone and each of us feels included, important and at ease. /p pThis job requisition is addressed also for candidates with disabilities and belonging to protected categories following articles 1 and 18, Law 68/99. /p h3Job Information /h3 ul liSeniority level: Mid‑Senior level /li liEmployment type: Full‑time /li liJob function: Quality Assurance /li liIndustries: Pharmaceutical Manufacturing /li /ul /p #J-18808-Ljbffr