At Thermo Fisher Scientific team, you’ll discover impactful job, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our products are safe. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our dedication to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building an exciting career with us. Ferentino, Italy | Quality: Discover Impactful Work: The resource will be part of a very stimulate environment and will ensure the respect of all quality standards requested by the norms in force, through the guidance, coordination, and control of the activities related to Sampling & Raw Materials, Microbiological and Digital QC areas. The role will develop & control assigned QC budget. In collaboration with the QA department, ensure the review of the Quality Agreements according to current EU GMP, US GMP and the client needs. Ensure the continued update of the operational procedures related to the QC area to align with the latest quality requirements. Verification of quality compliance, audit management, staff training, in respect of the norms in force (current EU GMP, US GMP), and Corporate Standards. Provides strategic vision and expertise for establishing and leading the Quality Control organization. Establishes department goals and objectives in line with Corporate and site goals. Leads all aspects of the people process including, hiring, on-boarding, performance management and employee development. Requirements: Education: - Scientific degree (e.g. FCT, Pharmacy, Chemistry, Biotechnology) Technical skills: - GMP - Regulatory knowledge - Knowledge of main analytical techniques Professional background: - Proven experience (about 5-8 years) in Quality departments in sterile pharmaceutical companies Languages: - Fluent English Personality Traits: - Steadiness - Leadership - Negotiation skills - Organizational skills