Job Description
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:
+ Set up, clean, and sanitize various manufacturing equipment.
+ Perform washroom activities for small and large-scale equipment.
+ Prepare buffers and media per manufacturing procedures (MPs) and SOPs
+ Monitor critical processes and perform basic troubleshooting.
+ Conduct in-process sampling and operate analytical equipment.
+ Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance.
+ Initiate quality reports.
+ Draft and revise SOPs and MPs.
+ Review documentation such as equipment logs and batch records.
+ Maintain ...
Responsibilities:
+ Set up, clean, and sanitize various manufacturing equipment.
+ Perform washroom activities for small and large-scale equipment.
+ Prepare buffers and media per manufacturing procedures (MPs) and SOPs
+ Monitor critical processes and perform basic troubleshooting.
+ Conduct in-process sampling and operate analytical equipment.
+ Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance.
+ Initiate quality reports.
+ Draft and revise SOPs and MPs.
+ Review documentation such as equipment logs and batch records.
+ Maintain ...
Ready to Apply?
Submit your application today and join our talented team at Quality Consulting Group.
Submit ApplicationJob Details
- Location Thousand Oaks, CA
- Job Type Full-time
- Category other-general
- Posted Date July 01, 2026
- Application Deadline July 05, 2026