JT030 - MCS 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:        Perform auxiliary tasks as needed (Batch Record Review, Closing Deviations, Document Revisions, Protein Concentration Testing).Prepare buffers and media per Manufacturing Procedures (MPs) and SOPsFollow GMP documentation (SOPs, MPs) with strict adherence to safety and compliancePerform and monitor critical processes, including basic troubleshootingConduct in‑process sampling and operate analytical equipmentExecute washroom activities, including cleaning small and large-scale production equipmentMaintain an organized and clean workspaceWork in a clean‑room environment while wearing steel‑toe shoes, full gowning, hairnet, and glovesAssist in reviewing documentation such as equipment logs and batch recordsIdentify, recommend, and implement improvements related to routine functionsPerform operations in the Manufacturing area, specifically for Purification processes.Qualifications:Bachelor’s degree or associate degree in related area4 years of Manufacturing experienceKnowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc.Prior manufacturing experience, basic AI knowledge, MS O365 knowledgeKnowledge of Single-use-SystemsCFR and Regulatory knowledgeAbility to interpret and apply GMP knowledgeBasic troubleshooting skills on production equipmentExperience with Delta VExperience with lab equipment/testingShift: 6:30 AM - 7:30 PM - Wednesdays - Saturdays week 1 of rotation (Thursdays - Saturdays week 2)Switches to graves every 6 months on rotationCandidates will start working day shift for the first 4-5 months and rotate with the team