PpDepartment: Corporate Quality Operations /p pJob Type: Direct Employee /p pBusiness Area: Quality /p pContract Type: Permanent /p pLocation: Parma, IT /p pbAbout us /b /p pChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here. /p pAt Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact. /p pDiversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better. /p h3bThis is what you will do /b /h3 pWithin the Global Quality Operations department, we are seeking an bOperational Compliance and Continuous improvement Lead /b to support and coordinate global activities and processes related to quality operations management of internal and external production including analytical processes. /p pThis role is pivotal in ensuring that a harmonized quality approach can be applied and driving continuous improvement initiatives. /p pThe role is based in Parma Italy, with a line report to the Global Operational Compliance Head. /p h3bYou’ll be responsible for: /b /h3 h3bIntegrated Quality operations Management: /b /h3 ul liCooperate with site quality representatives to ensure consistent quality of products manufactured across our Chiesi Farmaceutici SPA sites, respect and monitor the Quality KPI’s, support the application of quality Governance process and manage the main Global quality operation-related topics within the group, including handling of potential non‑conformities, deviations and change control. /li liSupport cascading guidelines and internal global SOPs providing support to the implementation at local level. /li liCooperate to guarantee compliance of the Validation processes and collaborate on drafting of Validation Project Plans and Validation Final Reports of the main internal projects. /li /ul h3bCross‑Site Support: /b /h3 ul liCollaborate closely with the Quality Directors representatives at each site to address common challenges (i.e. business continuity assessments, Corporate Audits, Inspection from Authorities). Support aligning quality processes and contribute the Quality Council and governance process at Local and Global Level (Tier1 and Tier 2). /li /ul h3bCollaboration with Compliance: /b /h3 ul liWork alongside the Compliance teams to support the process ensuring that quality standards meet internal and regulatory requirements. /li /ul h3bStrategic Leadership: /b /h3 ul liProvide support to the process to drive a culture of quality excellence throughout the organization. /li /ul h3bYou will need to have /b /h3 ul liMinimum of 10 years of experience in pharmaceutical quality assurance, with at least 5 years in a role with a proven track record in quality operations. Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector. /li liLeadership capabilities: Demonstrated ability to lead, influence, and collaborate with cross‑functional teams across multiple sites. Experience in change management and governance framework development. /li liExcellent communication skills: Outstanding relationship‑building skills, with the capacity to communicate complex quality issues clearly to various stakeholders. /li liStrategic thinking: Ability to analyze processes, foresee challenges, and implement effective solutions that enhance overall quality performance. /li /ul h3bIT Skills /b /h3 ul liProficient in Microsoft applications including Excel, Word, PowerPoint, Outlook and Teams. /li liAbility to use project management tools like Microsoft Project to plan, execute, and monitor quality‑related projects. /li liFamiliarity with software like TrackWise, or Veeva QualityDocs for managing quality documentation and processes. /li /ul h3bWhat we offer /b /h3 ul liNo matter where your path starts at Chiesi, it leads to inspiring possibilities. Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way. /li liWe provide top‑class benefits, including comprehensive healthcare programs, work‑life balance initiatives, and robust relocation support. Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options and tax assistance services for foreign colleagues, all designed to help you thrive. /li /ul pChiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business. All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination. /p /p #J-18808-Ljbffr