JT991 - ASSOCIATE MANUFACTURING

Quality Consulting Group • Holly Springs, NC

6d

About The Position

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.

Requirements

• High school diploma
• 1-2 years of work-related experience
• Biopharma Experience
• Experience in working in clean room
• GMP
• Dayshift
• 12 Hours Shift

Responsibilities

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED