LAVORO THE ASSESSMENT OF 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...

Languages fluency in english technical skills excellent knowledge of the clinical development settings...   who we are looking for purpose the clinical project management...

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

Who we are looking for purpose the utilities maintenance engineer will be the main point of contact with external providers, ensuring the management and control...

Ability to understand and evaluate multiple disciplines depending on the specificity of the opportunities under screening... purpose the redeo (r&d external opportunity)...

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...

these units are responsible for the development and implementation of the therapeutic area strategies... the intern will report to the gva global pricing sr analyst...

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

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...

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

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...

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

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

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...