JT844 - MCS MANUFACTURING ASSOCIATE

Thousand Oaks, CA

Temporary

Biopharmaceutical

Mid 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:

Perform hands-on operations including equipment setup, cleaning, and sanitization
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
Perform operations in the Manufacturing area, specifically for Purification processes.
Operations will be performed according to Standard Operating Procedures (SOPs) while complying with GMP standards in safe manner

Qualifications:

College degree (science-based preferred) Alternatively: Relevant industry or laboratory experience may be considered in place of a degree
Experience in biotech, pharmaceutical, or regulated manufacturing environments
Science-based background (laboratory, manufacturing, or related field)
Familiarity with: SOP adherence, GMP or GLP principles and General laboratory or manufacturing
Willing to commit to shift rotations.
Schedule: Day Shift or Graveyard Shift (12-hour shifts)
Day Shift: 7:00 AM – 8:00 PM or Graveyard Shift: 7:00 PM – 8:00 AM
Schedule Structure:
Front-half and back-half schedules
Includes alternating weekends off
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.

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