Quality Validation Associate Apply
A leading pharmaceutical manufacturer is seeking a Quality Systems & QC Laboratory Electronic Systems Administrator to support and maintain electronic quality and laboratory systems in line with GMP, GAMP, and data integrity requirements. This role will play a key part in ensuring systems such as electronic QMS and QC laboratory applications remain compliant, validated, and fit for purpose.ResponsibilitiesAdminister and support electronic QMS (e.g., TrackWise) and QC laboratory systemsSupport qualification and validation of equipment, processes, and electronic systemsMaintain user access, data integrity controls, and system availabilityCoordinate system updates, upgrades, and vendor support activitiesGenerate, review, and approve validation documentation and SOPsTroubleshoot system issues and provide user support and trainingRequirementsExperience supporting electronic QMS and/or QC laboratory systems in a GMP environmentWorking knowledge of CSV, GAMP, and data integrity principlesUnderstanding of qualification and validation for equipment and electronic systemsStrong analytical, documentation, and communication skillsComfortable working cross-functionally with IT, Quality, and external vendorsAbout Planet Pharma:Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information:E: fkeyworth@planet-pharma.co.uk

