JT272 - ASSOCIATE MANUFACTURING

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:        Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipmentPreparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)Following GMP documents (SOPs, MPs) with strict adherence to safety and compliancePerforming and monitoring critical processes with the ability to perform basic troubleshootingPerforming in-process sampling of equipment and operating analytical equipmentPerforming washroom activities: clean small- and large-scale equipment used in production activitiesWorking in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work Initiating quality deviation reports Drafting and revising documents (SOPs, MPs)Assisting in the review of documentation for assigned functions (equipment logs, batch records) Working around high-pressure systems and occasionally work around heavy equipmentQualifications:High school diploma + 2 plus years of biotech manufacturing experience specifically in upstream or downstreamBachelor’s degree in a science or engineering related major with no experience also consideredExperience in working in clean roomGMP KnowledgeAbility and desire to work in a fast-paced, hands-on, rapidly-changing environment. Every day will be different and most tasks are not repetitive. A lot of each shift is spent moving aroundFocused on Safety, Quality, and ComplianceMust have safety shoes. We can provide non‑prescription safety glassesThe schedule will be shifts (rotating 2-2-3, 12 hour shifts) on night shift rotation from 5:45pm to 6:15am