JT865 - MCS MANUFACTURING ASSOCIATE

Quality Consulting Group•Thousand Oaks, CA

28d•Onsite

About The Position

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.

Requirements

Bachelor’s degree or associate degree in related area
4 years of Manufacturing experience
Knowledge GMP Manufacturing & Process Execution - Core focus: Safe, compliant execution of manufacturing operations.
Experience in Quality, Compliance & Continuous Improvement - Core focus: Maintaining product quality and regulatory readiness.
Teamwork, Communication & Operational Readiness- Core focus: Reliable performance in a fast-paced manufacturing environment.
MUST be able commute to Thousand Oaks, CA

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
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