LAVORO REGULATORY AFFAIRS SENIOR PARMA, EMILIA ROMAGNA
(19 offerte di lavoro)
Listado de trabajos de Regulatory affairs senior en Parma, Emilia romagna
Senior global regulatory affairs project manager
Experience required 5 years in regulatory with good knowledge of drug development and regulatory procedures education at least bachelor’s degree in life sciences...
Senior clinical research physician non-obstructive respiratory diseases
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... collaborate with clinical program leaders, statisticians, regulatory...
Senior scientist - in vitro pharmacology - respiratory targeted drug discovery
It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...
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... engage with regulatory authorities, external experts, and key...
Clinical research physician copd/bronchiectasis
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...
Principal extractable and leachable scientist
Stay updated with the latest industry trends and regulatory changes... support to commercial manufacturing division in answering questions from regulatory...
Head of clinical project management
Ensure cpms maintain compliance with internal sops, gcp, and regulatory standards... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements...
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Modeling & simulation scientist
Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...
Head of global complaints, product quality risk & incident management
In-depth knowledge of regulatory requirements and industry standards related to product quality and complaints management (e... ensurs that all escalations are documented...
Intern - computational jr chemist / bioinformatician
Participating in the analysis and interpretation of computational results, under the guidance of senior scientists... it is divided into integrated functional areas...
Responsabile sviluppo prodotti elettromedicali
· collaborerai con marketing, quality, operations e regulatory affairs per garantire che le specifiche tecniche siano allineate alle esigenze del mercato e alle...
Responsabile sviluppo prodotti elettromedicali (ann401783)
· collaborerai con marketing, quality, operations e regulatory affairs per garantire che le specifiche tecniche siano allineate alle esigenze del mercato...
Vuoi trovare lavoro?
Vuoi trovare lavoro?
