LAVORO THE ROLE OF SCIENTIFIC PARMA, EMILIA ROMAGNA

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

Purpose the ideal candidate will be responsible for overseeing the global management of product complaints, coordinating the escalation process (girc), and supervising...

Who we are looking for purpose the clinical project management head is a senior leadership role within the clinical operations function, responsible for the line...

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

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

these units are responsible for the development and implementation of the therapeutic area strategies...   the franchise has full accountability for setting and...

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...

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...

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

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...

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

Assist in the management of intercompany agreements, including the preparation and review of standard contracts... main activities assist in the management of various...

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

We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... she/he will partner with customer facing...

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