LAVORO QUALITY REGULATORY ASSISTANT PARMA, EMILIA ROMAGNA
(28 offerte di lavoro)
Listado de trabajos de Quality regulatory assistant 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...
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...
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...
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...
Quality assurance specialist – master batch record - monza
Il profilo ricercato: il profilo ricercato possiede una laurea di ii livello in ambito scientifico (preferibilmente in ctf), ha maturato un'esperienza di 6 mesi/1...
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...
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...
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Participate to regulatory inspections and customer audits as required... develop and review quality documentation and procedures as requested...
Clinical research physician copd/bronchiectasis
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... outstanding communication skills with ability to interact with...
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...
Stay current with regulatory guidelines and industry trends related to patient engagement and innovation in clinical research... we strive to enhance patients’ well-being...
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...
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 clinical project management
Ensure cpms maintain compliance with internal sops, gcp, and regulatory standards... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements...
), to guarantee their quality and efficiency... therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality...
Sr. director, r&d external opportunities
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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