Computer Systems Validation (CSV) Specialist | Pharma (Hybrid)

Ambit Iberia
Sant Cugat del VallèsPresencialCompetitivoPublicado hace 19 díasSeniorIndefinidoRemoto: Híbrido
🇬🇧Inglés requeridoGamp5GxpValidationSopItil

Requisitos

Degree in Business Administration, Computer Science or comparable professional experience.
Proven experience in validation within a GxP-regulated environment, preferably in an IT area.
Strong knowledge of GAMP5 (v2) principles and their practical application.
Ability to quickly learn and manage lifecycle documentation (e.g., Validation Plan, URS, Functional Specifications, Risk Assessments, Test Reports, AAP, etc.).
Experience in developing and delivering training on KBs and SOPs aligned with the Validation Plan and AAP.
Familiarity with ITIL v4 is considered an advantage.
Excellent written and spoken English.
Proven ability to work effectively in a virtual, international, and multicultural environment.
Strong organizational, analytical, and problem-solving skills, with a results-driven mindset.
Excellent communication, collaboration, and stakeholder management skills.

Beneficios

Salary package based on your profile. We will discuss it on our first call.
Permanent Contract
Ticket restaurant included in-office hours
Flexible Retribution Program (Urban Sports Club)
Learning & Development 
Friend Referral Program

Anuncio original

We are looking for a Computer Systems Validation (CSV) Specialist to play a key role in ensuring compliance with regulatory requirements and internal standards by leading validation efforts throughout the system lifecycle. This position requires strong collaboration across cross-functional teams and a solid understanding of risk-based validation methodologies.

TASKS & RESPONSIBILITIES 🚀:


• Ensure that all validation activities are properly planned and executed in accordance with validation strategies, GxP requirements, and applicable BI SOPs prior to system go-live.
• Maintain the system's validated state throughout its lifecycle.
• Collaborate closely with Quality Assurance (QA) on compliance-related topics.
• Coordinate with System Owners, Process Owners, Business Process Owners, System Leads, Developers and other stakeholders.
• Ensure that all system-specific SOPs and System Lifecycle (SLC) documentation are in place before system operation.
• Oversee testing activities, including review and approval of executed test cases.
• Provide audit support and maintain up-to-date system documentation and presentations.
• Manage and resolve System discrepancies in collaboration with global system roles.
• Drive continuous improvement by optimizing and simplifying validation processes using risk-based approaches.

SKILLS 🤹:

• Degree in Business Administration, Computer Science or comparable professional experience.
• Proven experience in validation within a GxP-regulated environment, preferably in an IT area.
• Strong knowledge of GAMP5 (v2) principles and their practical application.
• Ability to quickly learn and manage lifecycle documentation (e.g., Validation Plan, URS, Functional Specifications, Risk Assessments, Test Reports, AAP, etc.).
• Experience in developing and delivering training on KBs and SOPs aligned with the Validation Plan and AAP.
• Familiarity with ITIL v4 is considered an advantage.
• Excellent written and spoken English.
• Proven ability to work effectively in a virtual, international, and multicultural environment.
• Strong organizational, analytical, and problem-solving skills, with a results-driven mindset.
• Excellent communication, collaboration, and stakeholder management skills.

SCHEDULE 🕘:

  • 08/09h -17/18h from Monday to Friday (flexible)

  • 4 days by remote & 1 day on-site

CONDITIONS 🌱:

  • Salary package based on your profile. We will discuss it on our first call.

  • Permanent Contract

  • Ticket restaurant included in-office hours

  • Flexible Retribution Program (Urban Sports Club)

  • Learning & Development 

  • Friend Referral Program

Our goal is that you are well in every way!

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