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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
