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.
Knowledge and experience in/with:
English (Minimum B2)
Spanish (Minimun B2)
Pharmaceutical Sector experience (GxP)
21 CFR Part 11 and EU GAMP Annex 11 regulations
GAMP 5
Computerized Systems Validations (CSV)
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
:
*****h -*****h from Monday to Friday (flexible)
Possibility of 100% remote working (Willingness and readiness to travel occasionally like the onboarding and every 3 months to visit the client)
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) - Spain based workers only. (available to candidates based in Spain only)
Discounts on gym network (Urban Sports Club) - available to candidates based in Spain only.
Learning & Development
Friend Referral Program
Our goal is that you are well in every way!