JT782 - ASSOCIATE MANUFACTURING NS

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:

• Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR] with strict adherence to safety and compliance
• Ensure proper gowning and aseptic techniques are always followed.
• Perform hands-on operation including set-up, cleaning, sanitization, monitoring of equipment and assigned area.
• Buffer and Media preparation and transfer. Weigh and dispense of materials to be used in the preparation of Buffers and Medias.
• Complete washroom activities: cleaning equipment, small to large scale, use in production activities.
• Run and monitor critical process per assigned procedures
• Perform documentation for assigned function (i.e., equipment logs, EBRs)
• Maintain an organized, clean, and workable space.
  

Qualifications: 

• High school diploma / GED 1 year of manufacturing and/or other regulated experience OR Associate’s degree
• Experience in a regulated industry such as biotechnology or pharmaceutical
• Basic understanding of GMP principles
• Strong verbal and written communication skills
• Proficient Microsoft Office skills
• Ability to follow detailed work instructions (SOPs)
• Initial schedule will be Monday-Thursday or Tuesday -Friday, 10 hours days
• The schedule will transition to shifts (rotating 2-2-3, 12 hour shifts) upon completion of startup activities and as business needs dictate