PbRD Analytical Scientist (Italia) page is loaded /b /ppRD Analytical Scientist (Italia) Apply locations Milan, Italy time type Full time posted on Posted Yesterday job requisition id R1473849 /ppOur client, Chiesi Farmaceutici – one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry - in order to expand their staff, entrusted to IQVIA the recruitment of an Analytical Scientist - Developing pharmaceutical products - who can join an exciting working environment in a dynamic and international atmosphere. /ppbJOB DESCRIPTION : /b /ppSupport analytical activities required for producing information and documentation suitable for preclinical and clinical development and registration of drug products, including excipients and intermediates, with particular focus on quality in accordance with GMP / cGMP. /ppbRESPONSIBILITIES : /b /ppDeveloping pharmaceutical products (small molecules, new chemical entities, biological products, excipients, intermediates, Drug Products) in line with QRM principles by designing and evaluating the necessary activities both internal and c / o CRO : /pullidevelopment, validation and transfer of analytical methods /lilistability studies set-up and management /lilidrug products characterization studies /liliextractables and leachables studies /lilistudies to support formulation and manufacturing process development (feasibility, refinement, scale-up,…) /liliExecute the development strategy of the assigned project /li /ulpContribute to the scientific understanding for the product development area /ppPreparation and revision of technical documentation in line with quality and regulatory requirements and according to relevant internal procedures /ppWriting / reviewing of regulatory documentation (CTD / NDA, IMPD / IND, QA, Briefing documents for Scientific advice) /ppOperate according to the related SOPs, cGMPs, safety guidelines and policies as necessary to accomplish daily tasks. /ppSupport Change Control Evaluation /ppSupport quality investigations (Deviations or OOS, Complaints) /ppbREQUIREMENTS : /b /pulliAt least 2 / 3 years of experience in a similar position in a pharmaceutical company or CRO. /li /ulpuTYPE OF CONTRACT : /u Permanent contract /ppbChemical contract /b /ppIQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with requirements responding to the open request. Applications WITHOUT the requirements Will NOT be fully taken into account. Please enter the authorization for the processing of personal data (DL196 / 2003) - General Data Protection Regulation (13 GDPR 679 / 16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.903 / 77). /ppbLI-CES #LI-DNP /b /ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at /ppbAbout Us /b /ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. /ppTo get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. /ppJ-18808-Ljbffr /p #J-18808-Ljbffr