LAVORO REGULATORY AFFAIRS COMPLIANCE PARMA, EMILIA ROMAGNA
(25 offerte di lavoro)
Listado de trabajos de Regulatory affairs compliance 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...
regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...
Engage with regulatory authorities, external experts, and key stakeholders to shape development plans and ensure compliance with global regulatory requirements...
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...
Clinical research physician copd/bronchiectasis
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... outstanding communication skills with ability to interact with...
regulatory compliance and safety: ensure that all maintenance activities and projects comply with current safety and environmental regulations, promoting a safe...
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 global quality life cycle
Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... main responsibilities integrated...
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Artwork development specialist - temporary
The role is based in parma (italy), in the global product compliance team... ); collect and conduct preliminary analysis of all information, data and files needed...
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...
Modeling & simulation scientist
Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...
Due diligence lead - temporary
Encompassing key areas such as global finance, global procurement, global ict, global human resources, global legal, compliance & ip, and global communications &...
Provide legal support to staff functions, sv&s, and chiesi foundation, including the possibility to draft operational legal notes and ensure legal compliance across...
Corporate quality auditing specialist - temporary
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...
Global r&d demand and business knowledge data scientist
It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...
Corporate quality auditing specialist
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...
Vuoi trovare lavoro?
Vuoi trovare lavoro?
