LAVORO MARKETS REGULATORY SME PARMA, EMILIA ROMAGNA
(24 offerte di lavoro)
Listado de trabajos de Markets regulatory sme 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...
Plant site process sme) on technical expertise for maintenance activities for in-market products, regarding maintenance needs collection, planning and execution...
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...
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... act as the main point of contact...
regulatory compliance and safety: ensure that all maintenance activities and projects comply with current safety and environmental regulations, promoting a safe...
Vuoi trovare lavoro?
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...
Artwork development specialist - temporary
To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the group researches, develops and markets...
Participate to regulatory inspections and customer audits as required... blois specializes in dry powder inhalers and final assembly stages of the metered-dose...
Head of global quality life cycle
Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... main responsibilities integrated...
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...
Collect information about new product launch and ensure the launch plan feasibility in terms of availability of the product coordinating all relevant stakeholders...
Corporate quality auditing specialist
Blois specializes in dry powder inhalers and final assembly stages of the metered-dose inhalers (mdis), supplies group’s affiliates and distributes directly to clients...
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?