Description
A leading pharmaceutical engineering consultancy is looking for a Qualification / Validation Engineer to support its growing portfolio of investment projects.This is a great opportunity to work on a diverse range of projects for leading global pharmaceutical organisations.
Location: Basel, Switzerland
Duration: 12 months +
Role and Responsibilities:
•Ensuring the compliance of new pharmaceutical production equipment and utilities on capital investment projects
•Writing and executing qualification protocols (DQ/IQ/OQ/PQ)
•Supporting client teams in the process validation phase of new production lines
•Ensuring a smooth handover from the engineering team to the client operations team
•Supporting the engineering team to ensure GMP compliance in all activities
Requirements:
•Degree educated in an engineering or scientific discipline
•Strong qualification experience within a pharmaceutical manufacturing environment
•Good GMP understanding
•Strong written and spoken communication skills - able to present information to clients
Apply now for the opportunity to work in one of Europe’s busiest pharmaceutical clusters.