Direct message the job poster from Philogen S.p.A.GMP Quality Assurance SpecialistPhilogen S.p.A. is looking for a GMP Quality Assurance Specialist who will report to the GMP Quality Assurance Manager and who will give his/her contribution to quality policies in support of Philogen’s Quality System.In particular the successful candidate will be responsible for:writing, reviewing and approving documents (SOPs, PQRs, IMPDs, validations, research reports, etc.);revision of production and quality control batch records;managing GMP QA operations, change control, deviation and documentation systems;identifying and recommending future improvements;implementing action plans;developing quality strategies and priorities and translating them into short and long-term objectives;interacting with other members of the company and clinical center staff.The ideal candidate should have:A good scientific background (ideally in Biology, Biotechnology, etc.)Previous experience in Quality Assurance (at least three years);Comprehensive knowledge of GMP and other regulations with a good understanding of global quality standards relating to product development, submission and clinical experimentation;A high level of English language, both written and spoken;A high level of attention to detail and with the ability to prioritize working tasks;A strong flexibility in changing tasks and priorities;The ability to work independently as well as coordinate members of his/her team;Excellent interpersonal skills and ability to work in teams.We offer:A contract and salary proportional to the experience of the successful candidate.Job location:SienaWe invite interested candidates to submit their applications expressly authorizing the processing of personal data in accordance with Legislative Decree 196/2003. Our recruitment adheres to the provisions of Legislative Decree 198/2006, and we welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief.Seniority levelAssociateEmployment typeFull-timeJob functionQuality AssuranceIndustriesPharmaceutical Manufacturing
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