Cleaning Validation Engineer - Pharmaceutical

Description

Pharmaceutical manufacturing plant, currently undergoing a large remediation project, has a contract requirement for an experienced CLEANING VALIDATION ENGINEER

Working for a US-owned company,that has recently purchased 4 manufacturing facilities, their aim is to get the plants up-and-running and qualified, towards manufacturing and FDA readiness

Due to a recent review of the VMP it has highlighted the need for an EXPERIENCED CLEANING VALIDATION Engineer to offer cleaning validation expertise and carry out the cleaning validation to the equipment

Pharmaceutical GMP experience is essential for this project.
Experience required:

• Cleaning Validation and qualification - IQ OQ PQ - Cip/Sip
• Ideally have worked on a pharmaceutical remediation project
• Pharmaceutical cGMP
• Created, reviewed and executed validation protocols - IQ OQ PQ
• We are looking for someone with excellent communication skills who are able to work with the local engineering teams to ensure that standards are met and work is carried out to a high standard

This is a hard working environment - 6 day/60 hour week. Not for the faint hearted! Flights, accommodation, £17.50/per dieme + food included and good hourly rate depending on your skills and experience. Initial 6 weeks on to get familiar and then 10 nights off (unpaid) rolling - 5 weeks on, 10 nights off.