LAVORO DESIGN DEVELOPMENT OF VALIDATION PARMA, EMILIA ROMAGNA
(18 offerte di lavoro)
Listado de trabajos de Design development of validation en Parma, Emilia romagna
Head of global quality life cycle
Supervise to guarantee the compliance of the validation processes and collaborate on the drafting of validation project plans and validation final reports...
Main responsibilities act as point of contact for gmd functions (incl... blois-la chaussée saint victor plant (france), a center of excellence specializing in the...
Device industrial development specialist
Il biotech center of excellence punta sull’innovazione biotecnologica, con particolare attenzione allo sviluppo di anticorpi monoclonali, enzimi e altre proteine...
Corporate quality auditing specialist - temporary
Preferred: experience in the manufacturing process of sterile medicinal products or inhalation products, and/or in the validation activities for the production of...
Global r&d demand and business knowledge data scientist
design and manage project cards to enable a standardized evaluation of business cases for pipeline projects and collaborate with bd to ensure consistency of treatment...
Basic knowledge of project management comprehensive understanding of drug development process... we strive to enhance patients’ well-being and quality...
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... education medical doctor degree from a renowned institution; certification...
Intern - global value and access - pricing jr analyst
Each franchise is organized by stage of development with fully empowered and enhanced teams of: pipeline development and commercial portfolio management...
Intern - computational jr chemist / bioinformatician
Basic knowledge of python (e... contributing to the automation of routine tasks in drug design workflows... participating in the analysis and interpretation of computational...
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Senior clinical research physician non-obstructive respiratory diseases
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... clinical section of the investigator’s brochure, protocols and clinical...
Principal extractable and leachable scientist
Deep knowledge of gmp/cgmp and guidelines (ich, emea, pqri, health canada) related to the pharmaceutical development of inhalation products...
Scientist - in vitro pharmacology - respiratory targeted drug discovery
Maintain detailed and accurate records of experiments and results... design, develop, and execute in vitro pharmacological assays to evaluate the efficacy and mechanism...
Review of temperature excursions and evaluation the subsequent suitability of the product for use... assist with investigations and management of the implementation...
Intern - corporate quality auditing
We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... blois-la chaussée saint victor plant...
Intern - patient advocacy eu & int
Maintain accurate documentation of activities and patient interactions... main activities as a patient advocacy intern, you will: support the design and execution...
Vuoi trovare lavoro?
Vuoi trovare lavoro?