Computer System Validation Consultant
Company: Jobbit
Location: Roma (zona Laurentina), Italy
Work hours: Full time 40 hours per week, Monday to Friday.
Contract: Initial 12‑month fixed‑term with a possibility to transition to permanent; CCNL Commercio, 14 monthly payments; pay commensurate with seniority.
Job Summary: This role focuses on ensuring that computerised systems used in regulated environments—pharmaceutical, medical, biotechnological, and chemical—are compliant, safe, and well documented.
Responsibilities

Support operational work directly in the field for equipment and cleaning validation and related documentation.
Write validation protocols and perform verification tests in controlled contamination environments.
Write protocols and execute IQ (Installation Qualification), OQ (Operational Qualification) tests for pharmaceutical equipment and facilities.

Qualifications

At least 4 years of experience in a similar role, preferably with a consulting firm.
Knowledge of reference regulations (US, EU) and pharmaceutical industry regulations.
Technical/scientific educational background.
Understanding of pharmaceutical processes.
Proficiency in drafting and reviewing technical and validation documentation.
English language ability.
Ability to work independently and in a team.
Attention to detail, precision and method.
Driver’s licence B.
Willingness to travel domestically and internationally for short trips.

Benefits

On‑the‑job and classroom training on technical topics and soft skills.
Language training budget.
Flexible hours.
Collaborative environment.
Possibility to work remotely.

Seniority Level
Mid‑Senior level
Employment type
Full‑time
Job function
Quality Assurance
Industries
IT Services and IT Consulting
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