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Gmp quality assurance specialist

Siena
Philogen S.p.A.
Pubblicato il 29 ottobre
Descrizione

PpDirect message the job poster from Philogen S.p.A. /ppbGMP Quality Assurance Specialist /b /ppPhilogen S.p.A. is looking for a bGMP Quality Assurance Specialist /b 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. /ppbIn particular the successful candidate will be responsible for: /b /pulliwriting, reviewing and approving documents (SOPs, PQRs, IMPDs, validations, research reports, etc.); /lilirevision of production and quality control batch records; /lilimanaging GMP QA operations, change control, deviation and documentation systems; /liliidentifying and recommending future improvements; /liliimplementing action plans; /lilideveloping quality strategies and priorities and translating them into short and long-term objectives; /liliinteracting with other members of the company and clinical center staff. /li /ulpbThe ideal candidate should have: /b /pulliA good scientific background (ideally in Biology, Biotechnology, etc.) /liliPrevious experience in Quality Assurance (at least three years); /liliComprehensive knowledge of GMP and other regulations with a good understanding of global quality standards relating to product development, submission and clinical experimentation; /liliA high level of English language, both written and spoken; /liliA high level of attention to detail and with the ability to prioritize working tasks; /liliA strong flexibility in changing tasks and priorities; /liliThe ability to work independently as well as coordinate members of his/her team; /liliExcellent interpersonal skills and ability to work in teams. /li /ulpbWe offer: /b /ppA contract and salary proportional to the experience of the successful candidate. /ppbJob location /b: /ppSiena /ppWe 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. /ph3Seniority level /h3ulliAssociate /li /ulh3Employment type /h3ulliFull-time /li /ulh3Job function /h3ulliQuality Assurance /li /ulh3Industries /h3ulliPharmaceutical Manufacturing /li /ul /p #J-18808-Ljbffr

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