Process & Computer System Validation Specialist (GCP)

3 giorni fa


Siena, Italia Philogen S.p.A. A tempo pieno

Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti-tumor therapies, is looking for a highly motivated and qualified Process & Computer System Validation Specialist (Gcp)RoleThe resource will join the QA department and will be responsible for the validation and maintenance of the company’s computerized systems, ensuring compliance with GMP/GCP regulations and quality standards. The role will be pivotal in QA GCP activities, contributing to process compliance and safeguarding data integrity in the clinical environment.Main Responsibilities- Validate and maintain computerized systems in line with GxP/GAMP best practices, with a specific focus on GCP. - Collaborate with QA and clinical teams to ensure quality and data integrity. - Manage validation documentation and draft/review SOPs related to computerized systems and equipment. - Participate in internal and external audits concerning validation and QA GCP activities. - Provide technical support and contribute to internal training on computerized systems.Requirements- Degree in technical/scientific disciplines. - At least 2 years of experience in the pharmaceutical sector, preferably with exposure to GCP activities. - Knowledge of the computerized systems lifecycle and experience with IQ/OQ/PQ qualifications. - Solid understanding of regulatory frameworks: FDA 21 CFR Part 11, EU Annex 11, ISPE GAMP, MHRA, PIC/S. - Good command of spoken and written English.Soft Skills- Ability to work effectively in multidisciplinary teams. - Proactivity, problem-solving skills, and result orientation. - Flexibility, passion for innovation, and strong commitment to quality and safety.



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