Process & Computer System Validation Specialist (GCP)

K-ARRAY | Unique Audio Solutions; San Pietro di Cadore; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading biotech company in Italy is looking for a highly motivated Process & Computer System Validation Specialist. This role involves validating and maintaining computerized systems, ensuring compliance with GMP/GCP regulations, and contributing to data integrity in clinical environments. Candidates should have a degree in a scientific discipline, at least 2 years of experience in pharmaceuticals, and a solid understanding of regulatory frameworks. A full-time position targeting associates offers a dynamic, quality-focused work environment.

Competenze

• At least 2 years of experience in the pharmaceutical sector, preferably with GCP exposure.
• Knowledge of 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.

Mansioni

• Validate and maintain computerized systems following GxP/GAMP best practices focused 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.
• Participate in audits concerning validation and QA GCP activities.
• Provide technical support and contribute to internal training on computerized systems.

Conoscenze

Teamwork

Problem-solving

Flexibility

Proactivity

Passion for innovation

Commitment to quality

Formazione

Degree in technical/scientific disciplines

Descrizione del lavoro

Process & Computer System Validation Specialist (GCP)

Direct message the job poster from Philogen S.p.A.

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)

Role

The 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.

• Seniority level: Associate
• Employment type: Full‑time
• Job function: Other
• Industries: Pharmaceutical Manufacturing

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