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
  • GAMP 5
  • Computerized Systems Validations (CSV)

Spanish and English (Minimum B2)

Good communication Skills

TASKS 🚀:
• 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.).

SCHEDULE 🕘:

• 08/09h -17/18h from Monday to Friday (flexible)
• Possibility of 100% remote working (Willingness and readiness to travel occasionally)

CONDITIONS 🌱:

• Salary package based on your profile. We will discuss it on our first call.
• Permanent Contract
• Flexible Retribution Program (medical insurance, public transport ticket and childcare check)
• Discounts on gym network(Andjoy)
• Learning & Development 
• Friend Referral Program

Our goal is that you are well in every way!