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 operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs). + Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment + Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs + Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance + Performing and monitoring critical processes with the ability to perform basic troubleshooting + Performing in-process sampling of equipment and operating analytical equipment + Performing washroom activities: clean small- and large-scale equipment used in production activities + Drafting and revising documents (SOPs, MPs) + Identifying, recommending, and implementing improvements related to routine functions + Assisting in the review of documentation for assigned functions (equipment logs, batch records) + Initiating quality reports Qualifications: + Associate’s degree + 6 months of related experience  + Mechanically inclined + Able to work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work + Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground. + Swing shift but workers must be flexible to work any shift (days, swings, graves) as workers will rotate every 3-6 months based on business needs + Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule 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. Powered by JazzHR