Jt025 - Mcs Manufacturing Associate

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:        

• Perform hands-on operations including equipment setup, cleaning, and sanitization specifically for Purification processes. 
• Prepare buffers and media per Manufacturing Procedures (MPs) and SOPs
• Follow GMP documentation (SOPs, MPs) with strict adherence to safety and compliance
• Perform and monitor critical processes, including basic troubleshooting
• Conduct in‑process sampling and operate analytical equipment
• Execute washroom activities, including cleaning small and large-scale production equipment
• Maintain an organized and clean workspace
• Work in a clean‑room environment while wearing steel‑toe shoes, full gowning, hairnet, and gloves
• Documentation & Quality
• Initiate quality reports
• Assist in reviewing documentation such as equipment logs and batch records
• Identify, recommend, and implement improvements related to routine functions

Qualifications:

• Bachelor’s degree or associate degree in related area (preferred)
• Alternatively: Relevant industry or laboratory experience may be considered in place of a degree
• Candidates with biotech or regulated industry experience are strongly preferred
• Reliable and punctual, Able to integrate quickly into a team environment, Comfortable with change and increasing production demands, Looking for hands-on manufacturing experience in a regulated setting
• Experience in biotech, pharmaceutical, or regulated manufacturing environments
  Science-based background (laboratory, manufacturing, or related field)
• Familiarity with: SOP adherence and GMP or GLP principles
• General laboratory or manufacturing best practices
• Schedule: Day Shift or Graveyard Shift (12-hour shifts)
• Day Shift: 7:00 AM – 8:00 PM
• Graveyard Shift: 7:00 PM – 8:00 AM
• Schedule Structure: Front-half and back-half schedules
• Includes alternating weekends off
• Onboarding: Initial training will take place on day shift
• Candidates will transition to assigned shift after training
   

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.