LAVORO REGULATORY AFFAIRS SPECIALIST PARMA, EMILIA ROMAGNA

Experience required 5 years in regulatory with good knowledge of drug development and regulatory procedures education at least bachelor’s degree in life sciences...

Proponiamo un’interessante opportunità come: master batch record specialist – sede: monza l’azienda nostra cliente è un’azienda globale leader nella produzione di...

); collect and conduct preliminary analysis of all information, data and files needed to prepare an artwork; technically analyze and verify the artwork, to ensure...

Who we are looking for purpose we are looking for a corporate quality auditing specialist to join our corporate team on a temporary contract...

Participate to regulatory inspections and customer audits as required... experience required previous experience in a similar role within the pharmaceutical...

Scopo il/la local master data specialist è responsabile della gestione e manutenzione dei dati master a livello di plant produttivo di san leonardo, assicurando...

Chiesi corporate functions these are the functions supporting the business:  global hr global finance, procurement & it group legal & corporate affairs global...

Insert the change impact in the qms follow and execute the pre and post-implementation actions supporting the changes - participates in maintenance of quality statements...

regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     collaborate with clinical program leaders, statisticians, regulatory...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     engage with regulatory authorities, external experts, and key...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...       outstanding communication skills with ability to interact with...

Stay current with regulatory guidelines and industry trends related to patient engagement and innovation in clinical research... act as the main point of contact...

Stay updated with the latest industry trends and regulatory changes...     support to commercial manufacturing division in answering questions from regulatory...

Ensure cpms maintain compliance with internal sops, gcp, and regulatory standards... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements...

Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...

It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...