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:

• 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
• Execute assigned manufacturing support activities in accordance with approved SOPs, batch records, and cGMP requirements
• Support equipment setup, breakdown, changeovers, and cleaning activities
• Perform material staging, and movement of consumables and components
• Complete GMP documentation (batch records, logbooks, forms) accurately and in real time
• Maintain area readiness, including housekeeping, 5S, and visual management standards
• Identify and promptly escalate deviations, safety concerns, and abnormal conditions
• Participate in shift handoffs, daily huddles, and cross-functional communication
• Complete all required training and support continuous improvement initiatives as assigned

Qualifications:

• High school/GED + 2 years work experience or Associates degree and 6 months work experience
• Biopharma Experience
• Experience in working in clean room
• GMP Knowledge
• Dayshift
• 12 Hours Shift

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.