Job Description

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:        

• Following Good Manufacturing Practices (GMPs) and applicable regulations from the Code of Federal Regulations (CFRs).
• Reporting any discrepancies to the Team Leader or Production Supervisor to ensure quality standards and safety.
• Ensuring quality & compliance through a Right First-Time mentality.
• Receiving and preparing components for use in manufacturing.
• Moving Buffer and Media totes to and from storage and point of use.
• Use of pallet jacks and PIVs.
• Ensuring components and products are available for continuous operation.

Qualifications:

• High school/GED and 1 year of work or military experience OR​ Associates degree​
• Knowledge of maintaining GMP status of manufacturing equipment.
• Able for moving full and empty Buffer and Media totes to and from storage area and point of use.
• Performing exterior cleaning of equipment to be brought into clean room areas per procedure.
• Experience using computers or automated systems
• Experience with manufacturing documentation
• Experience in Biotech cross lateral could be anything with batch chemicals or chemical processing.
• Day shift - 6:30am-7pm (rotating shift, every other week) 2 days on 3 days off etc. (Candidate is expected to work weekends and holidays)

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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