Spiacenti, l'offerta non è più disponibile,
ma puoi eseguire una nuova ricerca o esplorare offerte simili:

System Engineer Vmware Senior

La LOG.IT s.r.l., società specializzata nell'integrazione dei dati e nello sviluppo di piattaforme tecnologiche, in grado di processare e rendere intellegibi...


Da Log.It Srl - Toscana

Pubblicato a month ago

Rme Technician

Descrizione Il team Reliability Maintenance Engineering (RME) è fondamentale ad Amazon per monitorare tutte le attività operative: è grazie a questo team che...


Da Amazon Italia Transport Srl - Toscana

Pubblicato a month ago

Csv Specialist - Pharma Industry

Job description CSV SPECIALIST - PHARMA INDUSTRY Cosa farai? Eseguire attività di Validation dei sistemi informatici (CSV) relative ai sistemi di produzione....


Da Amaris Consulting - Toscana

Pubblicato a month ago

Software Engineer

TXT Group è alla ricerca di un dinamico Software Engineer da inserire nel nostro team di sviluppo di sistemi embedded. In qualità di Software Engineer, sarai...


Da Txt E-Solutions Spa - Toscana

Pubblicato a month ago

Gmp Quality Assurance Specialist

Gmp Quality Assurance Specialist
Azienda:

Philogen



Funzione Lavorativa:

Informatica

Dettagli della offerta

Job Title: GMP QUALITY ASSURANCE SPECIALISTDepartment: QAPhilogen 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, validation protocols and reports, technical reports, etc.);revision of production and quality control batch records;managing GMP QA operations, change control, deviations, CAPA 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;writing and reviewing risk assessments;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 and manufacturing;Knowledge of regulations for submission and clinical trials of IMP is a plus;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 :SienaInterested candidates are kindly asked to send their Curriculum Vitae to the following e-mail address ******, specifying the job position of interest authorizing the process of personal data under Italian Legislative Decree 196/03 and General Data Protection EU Regulation (2016/679).#J-18808-Ljbffr


Funzione Lavorativa:

Requisiti

Gmp Quality Assurance Specialist
Azienda:

Philogen



Funzione Lavorativa:

Informatica

Built at: 2024-05-18T11:27:05.609Z