JT902 - 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:

Under general supervision, employee will 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.
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:

Bachelor’s degree in a science-related field is preferred, but candidates with relevant manufacturing experience will also be considered.
Team player who can work in a structured, fast-paced manufacturing environment.
Experience with large-scale purification processes, including chromatography, filtration, and pressurized equipment.
Candidates must be detail-oriented, open to feedback, and able to follow strict GMP documentation procedures.
Work around high-pressure systems and occasionally heavy equipment.
Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
Primary Shift: 7:00 AM – 8:00 PM to start
Rotating Shift: 7:00 PM – 8:00 AM (6-month rotations)
Weekend Work: At least one weekend day per shift.
Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule

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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