LAVORO REGULATORY AFFAIR SPECIALIST MEDICAL

Il tuo ruolocome regulatory affair specialist presso capgemini engineering sarai un elemento chiave nelle seguenti attività:creare e aggiornare la documentazione...

Il/la candidato/a opererà nella divisione regulatory affairs di una realtà chimico-farmaceutica con ampio portafoglio prodotti/fornitori/clienti, operante su mercato...

Base regulatory strategy recommendations on precedents and other regulatory    intelligence as well as regulations and guidelines...   minimum requirements/qualifications:...

Ensures that regulatory submission timelines are aligned with program level and company objectives... may serve as a regional\/local regulatory lead and point of...

What youll achieve as a quality assurance regulatory affairs (qara) specialist you will ensure the respect of the quality and regulatory standards throughout the...

Prepare site regulatory documents, reviewing for completeness and accuracy...   knowledge and ability to apply gcp/ich and applicable regulatory guidelines...

Prepare site regulatory documents reviewing for completeness and accuracy... knowledge and ability to apply gcp/ich and applicable regulatory guidelines...

regulatory affairs senior specialist... desideriamo entrare in contatto con candidat? con esperienza pluriennale nel ruolo maturata nel settore medical devices,...

Ottima opportunità nel team di regulatory e market access... gestire le attività di market access, analizzando le politiche di rimborso e i criteri di accesso al...

Nel dettaglio si occuperà di:redazione, revisione, aggiornamento e raccolta della documentazione componente il design history file, in accordo all'mdr 2017/745 e...

Familiarity with pharmaceutical product/process development, regulatory guidelines and experience in regulatory submissions (in particular cmc module 3 information...

Per importante azienda multinazionale operante nel settore dispostivi medici, siamo alla ricerca di un/una product specialist medical device _ italia l’attività...

Job description validation specialist (ftc 12 months) about the role: the validation specialist supports small molecule validation activities, ensuring compliance...

Your attributes and skills   ·      willingness to travel in the italian territory up to 80%; ·      passion for medical products and technology; ·      customer-focused...

Grafton lifescience* è un team dedicato a valorizzare le esperienze, le competenze e il potenziale dei candidati in ambito sales&marketing, clinical research, regulatory...

The medtronic clinical and regulatory solutions (mcrs) function provides global support for clinical studies across all business units... we recognize their contributions...

Deep knowledge of regulatory and ethical requirements related to scientific drug information and, where applicable, medical devices... follow @abbvie on  x,  facebook...

Previous experience in tenders (both technical and procedural aspects) in the medical device field... good knowledge of english language click on apply if this sounds...