Validation Technician

Ambit Iberia; Sevilla; A distancia; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical services company is seeking a Validation Technician to manage validation documentation and support implementations. The role requires strong GxP knowledge, over 4 years of experience, and provides flexible hours with a 100% remote option. This is a permanent contract offering a collaborative work environment.

Formación

• Over 4 years of experience in the sector.
• Experience in Facility Management and engineering.
• Experience conducting change controls for compliance.

Responsabilidades

• Generate validation documentation for projects.
• Support the execution of qualification protocols.
• Maintain validation status through periodic reviews.

Conocimientos

Experience in computerized systems validation

Strong communication skills

Knowledge of GxP

Advanced knowledge of Microsoft Office 365

Educación

University degree in Chemical Engineering or related field

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 services to a pharmaceutical company. The role involves managing validation documentation and supporting the implementation of new functionalities and systems.

Responsibilities

1. Generation of validation documentation (Validation Plan / Report, Risk Analysis, Qualification Protocols such as OQ, PQ).
2. Support in the execution of qualification protocols.
3. Maintenance of validation status (e.g., Periodic Reviews).
4. Plan and manage projects according to client requirements and applicable legal regulations to achieve strategic objectives.
5. Address queries to technicians and create validation documentation for projects.

Skills

• University degree with postgraduate or Master's studies in Chemical Engineering, Industrial Engineering, Chemistry, Biology, or Biotechnology.
• Over 4 years of experience in the sector.
• Experience in computerized systems validation, Facility Management, engineering, and Security.
• Knowledge of GxP (GMP, GDP) in the pharmaceutical sector.
• Experience conducting change controls to ensure compliance with 21 CFR Part 11 and EU GMP Annex 11.
• Knowledge of Data Integrity and GAMP.
• Advanced knowledge and use of Microsoft Office 365.
• Strong communication skills and fluency in English.

Schedule

Monday to Friday: 08:00 to 17:00 / 09:00 to 18:00 (flexible)

100% remote position, permanent contract.

Our goal is that you are well in every way!

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