QA Officer

Applications Manager - Quality Management SystemThis role is responsible for ensuring the overall hygiene and GMP compliance of the manufacturing site, overseeing batch release processes, supporting external and internal audits, and maintaining quality documentation.ResponsibilitiesSupervise the general conditions of hygiene of the premises subject to its managementContribute in assuring the validation/qualification status of the production site, equipment, training of personnel and management of quality documentationResponsible for the provisional release for the shipment of batchesWork in shift with other QA officers to oversight the production and quality control activitiesArchive and support in managing the site GMP documentation, review of batch records and assure the timely closure of the manufactured batchesContribute in maintaining the local quality system as per GMPs and corporate guidelines and in assuring the respect of the GMPs and Health Authorities requirements at local levelSupport the QP in the preparation of batch release documentsCollaborate in redaction of site GMP documentation and preparation and printing of batch documentationSupport during the external audits by the authorities and corporate auditsCollaborate in data compilation of Product Reviews, oversight on investigations and monitoring of resulting actions are checked and approvedParticipate to the self-inspections as per approved annual plan and to the external auditsBe responsible for the appropriate level of quality oversight during the GMP activities of the facility, verifying they are executed according to the applicable standards in manufacturing, quality control, distribution and quality processesMinimum QualificationsEducation: Scientific degree in Pharmacy, Chemistry or Biology1+ years of experience in a Quality departmentStrong affinity with and awareness of quality issuesGood organizational skills including attention to detailSolid knowledge of quality system (GMP) and basic knowledge of regulatory requirementsFluent English verbally and in writingWhy Novartis?Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Learn more here: and RewardsRead our handbook to learn about all the ways we’ll help you thrive personally and professionally: to Diversity & InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse teams that are representative of the patients and communities we serve.Job DetailsSeniority level: Entry levelEmployment type: Full‑timeJob function: Quality AssuranceIndustries: Pharmaceutical Manufacturing#J-18808-Ljbffr