JT944 - ASSOCIATE MANUFACTURING

Quality Consulting Group•Holly Springs, NC

25d

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
Previous GMP experience
Dependable execution of assigned tasks in a shift-based, fast-paced environment
Clear verbal and written communication with operators, supervisors, and support teams
Willingness to learn, adapt, and work effectively within cross-functional manufacturing teams
Available for all shifts

Responsibilities

Hands-on support to daily manufacturing operations by executing assigned tasks in accordance with cGMP requirements, site SOPs, and safety standards
Support equipment readiness, material movement, documentation, and area maintenance to ensure safe, compliant, and efficient manufacturing operations
Execute assigned manufacturing support activities per approved SOPs, batch records, and cGMP requirements
Support equipment setup, breakdown, changeovers, cleaning, and sanitization activities
Perform material staging, movement, and reconciliation of consumables and components
Accurately complete GMP documentation (batch records, logbooks, forms) in real time
Maintain manufacturing area readiness, including housekeeping, 5S, and visual management standards
Identify, document, and promptly escalate deviations, discrepancies, safety concerns, or abnormal conditions
Participate in shift handoffs, daily huddles, and cross-functional communication
Complete all required training and comply with safety, quality, and data integrity expectations
Support continuous improvement initiatives as assigned