Would you like to work in a global, multicultural and multilingual team? We are looking for a "Validation Technician" who will offer service to a pharmaceutical company. Managing Validation Documentation and support the implementation of new functionalities/systems.

Responsibilities 🚀: 

• Generation of validation documentation (Validation Plan/Report, Risk Analysis, Qualification Protocols: e.g. OQ, PQ).
• Support in the execution of qualification protocols.
• Maintenance of validation status: execution (e.g. Periodic Reviews).
• Plan and manage projects, according to client requirements and applicable legal regulations, in order to achieve the company’s strategic objectives.
• Address queries to technicians and create validation documentation for the projects you lead.

SKILLS 🤹:

• University degree with postgraduate or Master's studies (Chemical Engineering, Industrial Engineering, Chemistry, Biology, 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 in 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 office software: Microsoft Office 365
• Strong communication skills.
• Fluent in English.

SCHEDULE 🕘:

• From Monday to Friday: 08 am to 17 pm / 09 am to 18 pm (flexible)
• 100% remote position
• Permanent Contract

Our goal is that you are well in every way!