Science Solutions are currently working with a Pharmaceutical Manufacturer in the West County who are looking to recruit a Validation Manager in a newly created position within the company.
As a Validation Manager you will have overall responsibility for Validation and Qualification activities across the site including the opportunity to develop, implement and maintain the site Validation Master Plan and Cleaning Validation Master Plan.
Responsibilities
Define and maintain the Site Validation Master Plan and Cleaning Validation Master Plan
Author, execute and report all qualification and validation activities across site.
Use Quality Risk Management principals to establish a risk based approach to validation
Lead the investigation and resolution of non-conformances encountered during validation, qualification and periodic review activities
Act as Validation SME during regulatory and customer inspections
Requirements
Significant experience of full life cycle validation activities with a GMP accredited Pharmaceutical/Medical Device environment including process, equipment, facilities, computer system and cleaning validation
Significant hands on experience authoring and executing validation and qualification protocols including URS, DQ, FAT, SAT, IQ, OQ and PQ
Line Management experience of a validation team is highly desirable
