LAVORO DIRECTOR OF THE SCIENTIFIC PARMA, EMILIA ROMAGNA

Proven scientific and drug development experience in multiple functions of the pharmaceutical industry...    ability to understand and evaluate multiple disciplines...

Supervise to guarantee the compliance of the validation processes and collaborate on the drafting of validation project plans and validation final reports...

Preferred: experience in the manufacturing process of sterile medicinal products or inhalation products, and/or in the validation activities for the production of...

Support the definition and periodic refresh of the r&d strategy through the collection and elaboration of both qualitative and quantitative information...

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...

Complementing these functions, the transformation office is responsible for ensuring the strategic alignment of the organization... ) to inform the assessments supports...

Purpose of the role: improving the lives of patients through innovative clinical research...      basic knowledge of project management    comprehensive understanding...

Excellent knowledge of the clinical trials settings...  innovation: work with relevant internal and external stakeholders to assess the use and implementation of...

Clinical section of the investigator’s brochure, protocols and clinical study reports)... they will drive the preparation of documents for regulatory submissions...

the role is based in parma (italy), in the global product compliance team... we believe that the success of chiesi is built and shaped by our people and our strong...

Purpose the intern will be in introduced in a dynamic and fast paced environment with the opportunity to support the activities of the corporate quality auditing...

Participating in the analysis and interpretation of computational results, under the guidance of senior scientists... basic knowledge of python (e...

the cpl  ensures scientific and medical integrity in the development and execution of clinical studies, leading clinical inputs into regulatory submissions and interactions...

Challenge the numbers...   the production area of officine farmaceutiche di parma is the main strategic hub for the production and distribution of chiesi products...

Clinical section of the investigator’s brochure, protocols and clinical study reports)... they ensure scientific and medical integrity in the development and execution...

Review of temperature excursions and evaluation the subsequent suitability of the product for use...     assist with investigations and management of the implementation...

Good knowledge of the univariate and multivariate (pca, doe) statistic...     deep knowledge of gmp/cgmp and guidelines (ich, emea, pqri, health canada) related...

Stay current with the latest scientific literature and technological advancements in the field of preclinical drug discovery... design, develop, and execute in vitro...