Quality Consulting Group Inc is hiring: JT210 - ASSOCIATE MANUFACTURING PROCESS

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 equipmentWeighing out 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 parts washing and sterilization activitiesMaintaining an organized and clean workspaceInitiating and being involved quality deviation reports, as requiredDrafting and revising documents (SOPs, MPs)Identifying, recommending, and implementing improvements related to routine functionsAssisting in the review of documentation for assigned functions (equipment logs, batch records)Working around high-pressure systems, occasionally work around/moving heavy equipment with powered industrial vehiclesChampion Lean Transformation and OE initiatives; facilitate the drive towards continuous improvement in all Manufacturing areas.Support DI&B initiatives to increase inclusion, connectivity, and engagement within the teamQualifications:Bachelors degree or Associate degree1-3 years work experience in manufacturing or operations.Experience working in a team.Comfortable handling chemicals or can demonstrate the importance of lab safety.Able to work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all workExperience with Systems MS office suiteGood written communicationExperience with troubleshooting (does not need to be biotech)Available to work various shifts (day/nights) as dictated by the production schedule Able to work in teams to complete operational tasksNight Shift 6:45PM - 6:45AMC and D Rotation - Swing Shift - Week 1 is 5 working days Week 2 is 2 working days. Candidates must be available to work weekends.Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.