LAVORO QUALITY SYSTEM COMPLIANCE REGULATORY PARMA, EMILIA ROMAGNA
(13 offerte di lavoro)
Listado de trabajos de Quality system compliance regulatory en Parma, Emilia romagna
Head of global quality life cycle
Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... main responsibilities integrated...
Corporate quality auditing specialist - temporary
The collaborator will be specialized in: - carrying out gxp/iso audits of gmd contractors in full authonomy, - drafting quality agreements, - ensuring supplier...
Corporate quality auditing specialist
Previous activity as supplier quality assurance... who we are looking for purpose the collaborator will be specialized in: - carrying out gxp/iso audits of gmd...
Intern - corporate quality auditing
Purpose the intern will be in introduced in a dynamic and fast paced environment with the opportunity to support the activities of the corporate quality auditing...
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...
), to guarantee their quality and efficiency... photovoltaic practices management: coordinate administrative and regulatory practices for photovoltaics, interfacing...
Artwork development specialist - temporary
The role is based in parma (italy), in the global product compliance team... experience required 1-2 years in the pharmaceutical industry, experience in quality...
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...
Vuoi trovare lavoro?
Stay current with regulatory guidelines and industry trends related to patient engagement and innovation in clinical research... we strive to enhance patients’ well-being...
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...
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...
Vuoi trovare lavoro?
Vuoi trovare lavoro?
