Computer System Validation Consultant

Jobbit; Roma; Ibrido; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A consulting firm in Italy is looking for a Computer System Validation Consultant to ensure compliance of computerised systems in regulated industries such as pharmaceuticals and biotechnologies. The role involves supporting operational work, writing and executing validation protocols, and understanding regulatory standards. Candidates should have a technical background, preferably 4+ years of experience, and possess strong attention to detail. Benefits include flexible hours and training opportunities.

Servizi

On-the-job and classroom training

Language training budget

Flexible hours

Collaborative environment

Possibility to work remotely

Competenze

• 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.
• Understanding of pharmaceutical processes.
• Driver's licence B.
• Willingness to travel domestically and internationally for short trips.

Mansioni

• Support operational work directly in the field for equipment and cleaning validation.
• Write validation protocols and perform verification tests.
• Execute IQ (Installation Qualification) and OQ (Operational Qualification) tests.

Conoscenze

Attention to detail

Proficiency in drafting technical documentation

Experience with regulatory compliance

Ability to work independently

Team collaboration

English language ability

Formazione

Technical/scientific educational background

Descrizione del lavoro

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