Requirements: English
Company: TN Italy
Region: Parma , Emilia-Romagna
Social network you want to login/join with:Head of Global Site Product Life Cycle, Parmacol-narrow-leftClient:Chiesi GroupLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:4523f835c086Job Views:1Posted:07.05.2025Expiry Date:21.06.2025col-wideJob Description:About usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with over 85 years experience, operating in 30 countries with more than 6,000 employees (Chiesi Group). To achieve its mission of improving peoples quality of life by acting responsibly towards society and the environment, the Group researches, develops and markets innovative drugs in its main therapeutic areas:We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification , a recognition of high social and environmental standards . We are a reliable company that adopts and promotes a transparent and ethical behavior at all levels.We believe that the success of Chiesi is built and shaped by our people and our strong set of shared Values and Behaviors . Our people make a critical difference to our success, which is why it is vital that we attract and retain the right talent who will continue to enrich our culture by living and breathing our values and behaviors.We are committed to embrace diversity, inclusion and equal opportunities. In fact, we are a global family made up of different cultures, different genders, generations, ethnicities, abilities, sexual identities and many other enriching diversities.Chiesi Global Manufacturing DivisionChiesi Group has three production plants:Parma (Italy), the strategic hub for the production and distribution of our products, serving as an international supply center with exports to over 80 countries. Here, solid medicines such as tablets and dry powders for inhalers, solutions and suspensions for inhalations and sterile suspension vials for endotracheal administration are produced.In 2024, a new Biotech Centre of Excellence has launched in Parma. The new facility is dedicated to developing and producing monoclonal antibodies, enzymes, and other proteins.Blois-La Chausse Saint Victor plant (France), a center of excellence specializing in the production of Dry Powder Inhalers and Metered Dose Inhalers (MDIs). The site manages direct distribution to customers in the French market and exports to other markets, effectively meeting both local and international needs.Santana de Parnaiba (Brazil), specialized in the production of pressurized solutions and suspensions for inhalation therapy (pMDIs). Additionally, it has an area dedicated to nasal sprays for the European market. Santana produces pressurised solutions and suspensions for inhalation therapy (MDI).In 2025, a new investment in Nerviano (Italy) has been announced with the construction of a new facility which will be primarily dedicated to manufacturing carbon minimal inhalers (reinforcing the companys commitment to both patients health and sustainable healthcare solutions), dry powder inhalers and sterile biological products.PurposeWithin the Global Quality Operations department, we are seeking a Life Cycle Quality Head to lead and oversee quality operations management across our manufacturing facilities and laboratories. This role is pivotal in ensuring a harmonized quality approach and driving continuous improvement initiatives across all sites.The role is based in Parma Italy, with a line report to the Global Quality Operations Vice president and has the report of a small team. The main focus is the Global Quality operations oversight and harmonization.Main ResponsibilitiesIntegrated Quality operations Management: Support to oversee and ensure the consistent quality of products manufactured across our Chiesi Farmaceutici SPA sites, to respect the Quality KPIs and to manage all Global quality-related topics within the group, including the handling of potential non-conformities, deviations and change control. Support to establishes guidelines for the validation of systems and processes according to national and international GMP regulations. Supervise to guarantee the compliance of the Validation processes and collaborate on the drafting of Validation Project Plans and Validation Final Reports. Set goals and timelines, evaluate data, and coordinates corrective actions.Cross-Site Coordination: Collaborate closely with the Quality Directors at each site to address common challenges (i.e. business continuity assessments, Corporate Audits, Inspection from Authorities). Support to align quality process and to coordinate the Quality Council at Local and Global Level (Tier1 and Tier 2)Collaboration with Compliance: Work alongside the Compliance teams to ensure that quality standards meet internal and regulatory requirements.Strategic Leadership: Provide strong leadership and guidance to drive a culture of quality excellence throughout the organization.Experience RequiredMinimum of 15 yea