Save Job Back to Search Job Description Summary Similar JobsWork in a role where you can have direct impact on business outcomesCompetitive package and career progression opportunitiesAbout Our ClientOur client is a Pharmaceutical Manufacturer based in Hertfordshire, who have a GMP accredited primary manufacturing site.Job DescriptionDevelop and execute validation protocols for equipment, processes, and systems.Ensure all validation activities comply with regulatory requirements and internal quality standards.Maintain detailed documentation of validation activities and results.Collaborate with cross-functional teams to support validation projects.Identify and address potential risks during validation processes.Provide technical support and guidance to ensure smooth implementation of validation strategies.Conduct regular reviews and updates of validation procedures as needed.Support audits and inspections by providing validation documentation and expertise.The Successful ApplicantA successful applicant will have:Knowledge of various validation activities, including cleaning, process, computer systems and equipment validationAbility to be adaptable and work to deadlinesConfidence to work independentlyWhat's on OfferPermanent position based in HertfordshireOpportunity to work in a small and agile Pharma businessAdditional benefits to be confirmed upon offerContactJames HarrisQuote job refJN-032026-6960036Phone number+44 113 243 7738Job summaryJob functionLife SciencesSubsectorQualitySectorHealthcare / PharmaceuticalLocationHertfordshireContract typePermanentConsultant nameJames HarrisConsultant phone+44 113 243 7738Job referenceJN-032026-6960036
