Intermediate Validation Engineer

The ideal candidate should have an engineering or science degree with a minimum of 5 years of industrial experience to include validation. Responsibilities include providing validation services to major pharmaceutical companies. The work may include all or part of the following activities: Design services for various utilities, equipment, and systems for manufacturing and packaging within cGMP environment. Support services for special assignments and projects ranging from manufacturing and packaging equipment to application software testing, installation qualification (IQ), operational qualification (OQ), performance qualification (PQ) protocols, standard operating procedures (SOP), installation, commissioning, factory acceptance tests (FAT), site acceptance tests (SAT) and training.
Requirements:Knowledge and experience to recommend and implement validation procedures professionally interact with clients and the ability to work as a team are required.

University degree in Chemical Engineering, Electrical Engineering, Computer Engineering or a directly related science discipline
A minimum of 3 years of relevant pharmaceutical validation experience, preferably in computerized system validation and automation systems e.g. Process Control systems
Familiarity with various pharmaceutical manufacturing and packaging systems, clean utilities, cleaning validation
Knowledge of GMPs and GAMP
Computer fluency and excellent knowledge of MS Tools, e.g. Office, Excel, MS Project
Availability to travel for short or extended stays
Valid passport and driver's licence
REQUIREMENTS
See Above / gj-hh