We are looking for a “Validation Technician” who will offer service to a pharmaceutical company. Managing Validation Documentation, in charge of multiple validation projects and their agendas.

SKILLS :

• University studies with postgraduate or Master’s degree (Chemical Engineering, Industrial Engineering, Biotechnology).
• Knowledge and practice of office automation at an advanced level: Microsoft Office.
• Desirable: 3 years or more experience in a similar position.
• Knowledge and experience in/with:
• Spanish and English (Minimum B2)
• Pharmaceutical Sector (GxP)
• 21 CFR Part 11 and EU GAMP Annex 11 regulations

• Definition of validation strategies.
• Generation of validation documentation (Validation Plan, Risk Analysis, Qualification Protocols: IQ, OQ, PQ, reports).
• Support and help to the staff that will be functionally in charge of it, for the revision of documentation.
• Management of the schedule of different projects under your responsibility for validations.
• Communication with the work team (project status, incidents detected, etc.).