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Validation engineer

Independent Solutions
Validation engineer
Posted: 11h ago
Offer description

An excellent opportunity has arisen for a Validation Engineer to support validation activities within a state-of-the-art pharmaceutical manufacturing facility focused on innovative vaccine manufacturing and product development.This role is ideal for candidates with broad validation experience across equipment, utilities, and facilities within GMP-regulated pharmaceutical or biotechnology environments.Key ResponsibilitiesSupport site validation activities across multiple workstreams.Assist with Environmental Monitoring Performance Qualification (EMPQ) strategies and maintenance of EM protocols/procedures for graded pharmaceutical areas.Support equipment qualification activities from Operational Qualification (OQ) through Process Performance Qualification (PPQ), including requalification/revalidation activities.Assist with regulatory submissions, audits, inspections, and site readiness activities.Participate in problem-solving and risk assessment initiatives.Drive continuous improvement and operational excellence activities.Support organizational initiatives related to safety, compliance, forecasting, and standardization.Maintain strong focus on GMP compliance, quality standards, and patient safety.Stay updated with scientific, technical, and regulatory developments.Requirements5 years’ experience within pharmaceutical or biotechnology validation environmentsStrong understanding of cGMP and regulatory requirementsBiological SciencesChemical EngineeringBiological Engineeringor related disciplinePreferred ExperienceFacility, utility, and equipment qualification including:CTUsParts WashersAutoclavesClean UtilitiesHVAC/CleanroomsExperience supporting:Upstream/downstream processesFill finish/formulation operationsTechnology transferProcess validation & PPQCommercial manufacturing readinessRegulatory documentation/CTD authoringAdditional InformationThis is a general validation engineering role with broad exposure across validation activities.Candidates do not need to be specialists in one particular validation area.Flexible/hybrid working may be considered depending on business needs.
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