LAVORO ANALYSIS OF THE COMPLEX 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...

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...

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...

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...

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

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

the members of kpmg’s ctr team support organisations across all phases of the process to ensure the security of their information and business strategies...

Provide clinical leadership within the core team, ensuring the clinical perspective informs key strategic decisions... we believe that the success of chiesi...

Facs analysis and immunology techniques... stay current with the latest scientific literature and technological advancements in the field of preclinical drug discovery...