JT255 - Associate Manufacturing Process Technician - NS

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 equipment
• Weighing out buffers/media per defined manufacturing procedures (MPs) and standard operating procedures 
• 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 parts washing and sterilization activities
• Maintaining an organized and clean workspace
• Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
• Assisting 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 vehicles
• Champion 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 team
• Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations
• 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

Qualifications:

• Associate degree OR High school with 3 years' work experience in manufacturing.
• Night Shift 6:45PM - 6:45AM
• C and D Rotation - Swing Shift - Week 1 is 5 working days Week 2 is 2 working days. (weekends)
• Experience in equipment preparation work for bioreactors running cleaning cycles gathering materials.
• Experience working effectively on a team, lab exposure and worked in an environment where safety is top priority.
• Manager is open to candidates that don't necessarily have experience in Biotech cross lateral could be anything with batch chemicals or chemical processing.

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.

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