JT025 - MCS MANUFACTURING ASSOCIATE

Quality Consulting Group•Thousand Oaks, CA

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 (preferred)
Alternatively: Relevant industry or laboratory experience may be considered in place of a degree
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
Familiarity with: SOP adherence and GMP or GLP principles
General laboratory or manufacturing best practices

Nice To Haves

Candidates with biotech or regulated industry experience are strongly preferred
Experience in biotech, pharmaceutical, or regulated manufacturing environments
Science-based background (laboratory, manufacturing, or related field)

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
Initiate quality reports
Assist in reviewing documentation such as equipment logs and batch records
Identify, recommend, and implement improvements related to routine functions