Validation Specialist (multiple area: Milano e Latina)

CSV Life Science Group, operating in the pharmaceutical sector, is looking for a Validation Specialist to be inserted within its own CQV team. The search is active on two sites: Milano and Latina. The resources will be involved in structured projects for the main players in the pharmaceutical industry and will be responsible for drafting and executing qualification protocols on site in accordance with predefined standards and ensuring compliance with reference regulations. The main responsibilities will include: • Developing and implementing validation protocols; • Conducting audits and inspections to ensure compliance with regulatory requirements; • Collaborating with cross-functional teams to identify and mitigate risks; • Providing training and support to team members; • Maintaining accurate records of all activities performed. The ideal candidate should have a degree in Life Sciences or related field, 3-5 years of experience in validation and quality control, knowledge of GMPs and GLPs, and proficiency in MS Office. The company offers a competitive salary, opportunities for professional growth, and a dynamic work environment.