LAVORO DEVELOPMENT OF MANUFACTURING PROCEDURES PARMA, EMILIA ROMAGNA
(19 offerte di lavoro)
Listado de trabajos de Development of manufacturing procedures en Parma, Emilia romagna
Head of clinical project management
Languages fluency in english technical skills excellent knowledge of the clinical development settings... main responsibilities line management & people development...
Head of global quality life cycle
Experience in change management and governance framework development... supervise to guarantee the compliance of the validation processes and collaborate on...
Head of global complaints, product quality risk & incident management
Preferred: management of teams (also in dotted line settings) with members based in multiple countries experience with sterile/aseptic manufacturing environments...
Artwork development specialist - temporary
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...
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...
Knowledge of project management techniques and procedures for managing company projects is also required... good knowledge of electrical systems and related safety...
Excellent knowledge of the clinical trials settings... innovation: work with relevant internal and external stakeholders to assess the use and implementation of...
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...
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Supply oversight of the delivery plan in order to grant the continuity of production plan, the right level of stock and escalating in case of risk/opportunities...
Principal extractable and leachable scientist
Collaborate with commercial manufacturing to perform risk assessment of perls... deep knowledge of gmp/cgmp and guidelines (ich, emea, pqri, health canada)...
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...
The new biotech centre of excellence for biological drug development and production will specialise in the development and production of active ingredients such...
Review of temperature excursions and evaluation the subsequent suitability of the product for use... assist with investigations and management of the implementation...
Main activities assist in the management of various types of agreements (e... assist in the management of intercompany agreements, including the preparation and...
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...
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Vuoi trovare lavoro?