Validation Technician for IT Automation | Pharma - Hybrid

Ambit Iberia; Sant Cugat del Vallès; Presencial; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical sector seeks a Validation Technician to ensure compliance with validation standards and maintain validated systems. This opportunity offers flexibility with remote work, permanent contract benefits, and a comprehensive salary package tailored to your profile.

Servicios

Permanent contract

Ticket restaurant for in-office hours

Flexible retribution program

Discounts on gym network

Learning & Development opportunities

Friend referral program

Formación

• Mandatory knowledge of the pharma industry and GxP standards required.
• Over 3 years of experience focusing on validation in a GxP environment.
• Experience supporting validation lifecycle documentation for LeVA systems.

Responsabilidades

• Ensure compliance with the validation plan and applicable standards.
• Maintain validated status of systems post-operation.
• Act as validation manager during the operational phase.

Conocimientos

Knowledge of pharma industry

GxP standards

Professional IT experience

Validation lifecycle documentation

Educación

Degree in Computer Science or comparable

Descripción del empleo

Would you like to work in a global, multicultural, and multilingual team? We are looking for a "Validation Technician" who will provide service to the Enterprise Service Management Platform (ServiceNow & UIPath) for one of our clients in the pharmaceutical sector.

Responsibilities

1. Ensure that appropriate validation activities take place to comply with the validation plan and applicable standards prior to system operation.
2. Ensure that all system-specific SOPs and SLC documentation are in place before the operation phase.
3. Maintain the validated status of the system after it becomes operational, acting as the validation manager of the system.

Skills

1. Degree in Computer Science or comparable professional experience.
2. Mandatory knowledge of the pharma industry and GxP standards.
3. Over 3 years of professional IT experience focusing on validation in a GxP environment.
4. Experience supporting lifecycle documentation for LeVA systems (e.g., VP, URS, FS, RA, Testing Reports, AAP) and developing/training applicable SOPs as per Validation Plans.

Schedule

• 08/09h - 17/18h from Monday to Friday (flexible).
• 1 day in-office | 4 days remote.

Conditions

• Salary package based on your profile; to be discussed during our first call.
• Permanent contract.
• Ticket restaurant included during in-office hours.
• Flexible retribution program (medical insurance, public transport ticket, childcare check).
• Discounts on gym network (Wellhub).
• Learning & Development opportunities.
• Friend referral program.

Our goal is that you are well in every way!