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: 3-5 years or more experience in a similar position, preferrable validating SAP

• Knowledge and experience in/with:

• Spanish and/or English (Minimum B2)

• Pharmaceutical Sector (GxP)

• 21 CFR Part 11 and EU GAMP Annex 11 regulations

• GAMP 5

• Computerized Systems Validations (CSV)

• 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 like the onboarding)

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!