JT398 - MANUFACTURING ASSOCIATE

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities:        Manufacturing support role responsible for manual visual inspection and packaging of post-inspected unitsManual visual inspectionInterface with GMP systemsUnder minimal supervision, performs manufacturing according to Standard Operating ProcedureOperate critical processing equipmentAssist in ensuring operations are completed per manufacturing scheduleResponsible for identifying and communicating problems during operationsReview, revise, and audit documentsPerform computer operations (MES, EBR, MAXIMO, LIMS and SAP Knowledge)Qualifications:Associate degree preferred1-year minimum GMP background manufacturing, computer savvy, SAP Knowledge is helpful as candidate will need to use Manufacturing Execution SystemExperience with manual visual inspection of drug product or in a GMP regulated environmentExperience with PAS X Werum software for electronic batch records with some understanding of editing and validationKnowledgeable of manual visual inspection or strong understanding of related disciplinary areas in bioprocessing (Drug Product operations)Require a passing eye exam, which includes colorThe current shift structure is 6am-3pmSome training does require an earlier start time of 4am/5amSome processes may require earlier shift start times and/or weekend work to meet production demandPossibility to move to graves/swing shift but job seekers should be flexible.