JT243 - ASSOCIATE MANUFACTURING

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:        

• 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
• Performing and monitoring critical processes with the ability to perform basic troubleshooting
• Performing in-process sampling of equipment and operating analytical equipment
• Performing washroom activities: clean small- and large-scale equipment used in production activities
• Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
•  Initiating quality deviation reports
•  Drafting and revising documents (SOPs, MPs)
• Assisting in the review of documentation for assigned functions (equipment logs, batch records)
•  Working around high-pressure systems and occasionally work around heavy equipment
  

Qualifications:

• High school diploma   2 plus years of biotech manufacturing experience specifically in upstream
• Completion of NC BioWork Certification Program preferred
• Experience in working in clean room
• GMP Knowledge
• Ability and desire to work in a fast-paced, hands-on, rapidly-changing environment. Every day will be different and most tasks are not repetitive. A lot of each shift is spent moving around
• Focused on Safety, Quality, and Compliance
• Must have safety shoes. We can provide non‑prescription safety glasses
• Must be flexible on the working hours
• Available to work various shifts
• Rotating 2-2-3 (5:45AM-6:15PM) 12 hours shifts