JT924 - 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:

  • Equipment set up, operating process equipment, buffer/media prep, equipment cleaning, sampling of in-process product pools and sample management in electronic sample management system, recording process data in systems
  • Under general supervision, employee will perform operations in the Manufacturing area.
  • Operations will be performed according to Standard Operating Procedures (SOPs) while complying with GMP standards in safe manner.
  • 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)Set up, clean, and sanitize manufacturing equipment.
  • Performing and monitoring critical processes with the ability to perform basic troubleshooting
  • Initiating quality deviation reports
  • Conduct in-process sampling and operate analytical equipment.
  • Execute washroom activities, including cleaning small- and large-scale equipment.
  • Maintain an organized, clean, and compliant workspace.

Qualifications:

  • Associates degree
  • Chromatography Experience - At least 1 year experience preferred - (protein separation)
  • Biotech Process Development or Manufacturing experience - downstream purification area (process development, clinical manufacturing, protein purification, cell culture)
  • Large Scale processing, buffer prep or media prep experience
  • Team switches every quarter (4x/year). New hire will remain on days for first 2-3 months and then may switch to swings or stay on days. Rarely will work graves (maybe 2x/ year).
  • All candidates must be open to working days and swing

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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