CSV Consultant (Lombardia)

fortil; Milano; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

An engineering and consulting group in Lombardia is seeking a CSV Consultant. The successful candidate will validate computerized systems in the Life Science sector, manage remediation projects, and draft validation documents. A Bachelor's or Master's degree in a relevant field and 3+ years of experience in CSV projects are essential. The role offers full-time employment focused on consulting, information technology, and sales. Join a dynamic team dedicated to professional growth and community involvement.

Servizi

Personalized support for skill growth

Encouragement to step outside comfort zone

Opportunity to become a shareholder

Involvement in community projects

Support policy for parenthood

Competenze

• 3+ years of experience on CSV projects in the Life Science field.
• Skilled in mapping data flows and performing gap analyses.
• Excellent knowledge of Office package required.

Mansioni

• Validate computerized systems in the Life Science sector.
• Manage remediation projects for computerized system adaptations.
• Draft validation documents and test protocols.

Conoscenze

Data flow mapping

Gap analysis

Good knowledge of GMP

Good knowledge of CFR 21 Part 11 Regulations

Fluent in English

Office package

Formazione

Bachelor's or Master's degree in technical‑engineering or related fields

Descrizione del lavoro

CSV Consultant (Lombardia)

Fortil is an international engineering and technology consulting group built on an independent model, bringing together over 2,500 employees. With 30 offices across 14 countries, Fortil fosters entrepreneurial freedom and the empowerment of individual potential.

Location: Lombardia.

Responsibilities

• Validation of computerized systems in the Life Science sector (e.g. laboratory instrumentation control systems, automation systems and quality systems - ERP, LIMS, DMS - according to the GxP reference regulations and GAMP Guidelines).
• Support in the management of remediation or requalification projects for the adaptation of computerized systems to the FDA 21 CFR part 11/EU Annex 11 regulations and to the Data Integrity regulations and guidelines.
• Periodic review of computerized systems and user audit trails.
• Drafting of validation documents: Validation Plans, URS, Traceability Matrices.
• Drafting and execution in the field of test protocols: IQ/OQ/PQ.
• Drafting of Risk Assessments.
• Drafting of computerized system administration procedures.

About You

• Bachelor's or Master's degree in technical‑engineering or similar subjects (Chemical Engineering, Chemistry, Industrial Chemistry, Mechanical Engineering, CTF, Pharmacy, Biology).
• 3+ years of experience on CSV projects in the Life Science field.
• Skilled in mapping data flows and performing gap analyses to identify compliance and process improvement opportunities.
• Good knowledge of the reference regulations and guidelines. In particular, knowledge of GMP, CFR 21 Part 11 Regulations, EU/GMP Annex 11, ISPE GAMP5; guidelines, data integrity regulations and guidelines (e.g. MHRA, WHO, EMA, FDA) and ICH guidelines, in particular ICHQ9, is required.
• Good knowledge of the English language, both written and spoken.
• Excellent knowledge of the Office package.

Why join us?

• Personalized support to help you grow your skills.
• An ecosystem that encourages you to step outside your comfort zone.
• The opportunity to become a shareholder.
• Involvement in community and non‑profit projects.
• A dedicated policy to support parenthood.

Fortil is committed to equal opportunity. All our positions are open to people with disabilities, regardless of gender, origin, or sexual orientation.

Seniority level

Mid‑senior level

Employment type

Full‑time

Job function

Consulting, Information Technology, and Sales

Industries

Business Consulting and Services