LAVORO QUALITY MANAGEMENT REGULATORY AFFAIRS PARMA, EMILIA ROMAGNA
(32 offerte di lavoro)
Listado de trabajos de Quality management regulatory affairs en Parma, Emilia romagna
Head of global complaints, product quality risk & incident management
quality management, engineering, life sciences)... in-depth knowledge of regulatory requirements and industry standards related to product quality and complaints...
Senior global regulatory affairs project manager
Align with project and portfolio management (ppm) to identify key milestones for gra to meet business objectives, from clinical trial initiation, regulatory submission...
Head of global quality life cycle
Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... experience in change management...
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...
Head of clinical project management
Understands financial procedures, budget management... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements, and cro/vendor management...
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...
regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...
), to guarantee their quality and efficiency... knowledge of monitoring and management systems for utilities... preferred skills: experience with photovoltaic...
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...
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Ensure quality risk management documentation is complete and maintained and assist with administration of the records retention programme...
Senior clinical research physician non-obstructive respiratory diseases
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... it is divided into integrated functional areas focusing on pipeline...
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... engage with regulatory authorities, external experts, and key...
Basic knowledge of project management comprehensive understanding of drug development process... it is divided into integrated functional areas focusing...
Intern - global value and access - pricing jr analyst
Education master’s degree in life sciences, health economics / economics, management engineering... each franchise is organized by stage of development with fully...
Intern - commercial business partner china & international
Help management team to identify opportunities and threats through analytics... each franchise is organized by stage of development with fully empowered and enhanced...
Principal extractable and leachable scientist
Stay updated with the latest industry trends and regulatory changes... it is divided into integrated functional areas focusing on pipeline projects including...
Modeling & simulation scientist
Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...
Artwork development specialist - temporary
Experience required 1-2 years in the pharmaceutical industry, experience in quality departments will be considered a plus education master’s degree, scientific (e...
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Vuoi trovare lavoro?
