JT991 - ASSOCIATE MANUFACTURING

Holly Springs, NC

Temporary

Biopharmaceutical

Entry Level

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:

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 diploma
1-2 years of work-related experience
Biopharma Experience
Experience in working in clean room
GMP
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.

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