Overview As QA Officer you ensure quality oversight across GMP activities at the site. You will support validation/qualification efforts, manage quality documentation, and supervise batch release activities. Working in shifts, you contribute to audits, inspections, and continuous improvement of the local quality system. This role offers exposure to cross-functional coordination and regulatory compliance in a integral pharma environment. You will partner with QP and QA colleagues to safeguard product quality and compliance.
Compensaciones / Beneficiosflexible and hybrid working optionsminimum of 14 weeks paid parental leaveinsurance plansretirement planswellbeing resourcesglobal recognition programs ResponsabilidadesOversee hygiene and facility conditionsSupport validation/qualification status, training, and quality documentationResponsible for provisional batch releaseCollaborate with QA officers to supervise production and QC activitiesArchive and manage GMP documentation, review batch records,
close batchesMaintain local quality system per GMP and corporate guidelinesAssist in batch release documents with QPContribute to drafting GMP documentation and batch documentationSupport data compilation for Product Reviews, monitor investigations and corrective actionsParticipate in self-inspections and external auditsEnsure quality oversight during GMP activities per standards in manufacturing, QC, distribution and quality processes Requisitos principales1+ years of experience in a Quality departmentStrong affinity with and awareness of quality issuesGood organizational skills with attention to detailSolid knowledge of GMP quality systems and basic regulatory requirementsFluent in English (spoken and written)CollaborationLeadershipOperational excellenceGMP knowledgeQuality system understandingRegulatory compliance awareness