LAVORO GLOBAL REGULATORY AFFAIRS SPECIALIST PARMA, EMILIA ROMAGNA

Support internal initiative(s) with a goal to accelerate internal regulatory processes and subsequently development timeline - in collaboration with the gra global...

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

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

The role is based in parma (italy), in the global product compliance team... in fact, we are a global family made up of different cultures, different genders, generations...

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

Chiesi global manufacturing division chiesi group has three production plants: parma (italy); blois-la chaussée-saint-victor (france); santana de parnaíba (brazil)...

Participate to regulatory inspections and customer audits as required...     chiesi global manufacturing division chiesi group has three production plants: parma...

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

Engage with regulatory authorities, external experts, and key stakeholders to shape development plans and ensure compliance with global regulatory requirements...

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...       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... it is divided into integrated functional...

Stay updated with the latest industry trends and regulatory changes... it is divided into integrated functional areas focusing on pipeline projects including...

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...