Smart4 Sciences are currently working with a GMP regulated Pharmaceutical Manufacturer to recruit a Validation Officer to their site in Hertfordshire

As a Validation Officer you be part of a small team responsible for maintaining the site Validation Master Plan and will be required to lead, author and perform IQ, OQ, PQ protocols including Process, Cleaning, Equipment and Computer Systems; completing all associated documentation in accordance with ICH guidelines and GMP standards.

Key Responsibilities

Lead, author and execute IQ, OQ, PQ protocols on specific projects including Process Validation, Cleaning Validation, Computer System Validation and Facilities Validation
Manage all validation documentation including commissioning test scripts, qualification/validation protocols, summary reports and risk assessments
Perform qualification reviews, identifying and implementing any remedial work required.Key Requirements

BSc or equivalent in a relevant life science or engineering discipline
Demonstrable experience of validation and qualification within the Life Science sector including working knowledge of GMP requirements for validation in the UK and/or EU.
Strong communication and project management skills including the ability to collaborate with colleagues at all levels.If you have prior experience in Validation and would be interested this position please apply to day or contact Gareth at Smart4 Sciences for more information