Build and maintain specifications in the ALEXIS LIMS system.
Build and maintain sessions in VelQuest Smartlab.
Administration of laboratory software systems.
Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as
Draft, review, and approve validation and qualification documentation for analytical software.
Draft, review, and approve SOPs, forms, and associated documentation with analytical equipment.

🎯 Requirements

Bachelor’s Degree or above in Chemistry or related Science
3-5 years relevant Quality Control experience or equivalent combination of education and experience
Experience in pharmaceutical manufacturing facility.
Demonstrate knowledge of cGMP requirements and practices including extensive knowledge of the USP
Demonstrate competency in review of data generated by QC laboratory as attention to detail is a

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Engineering Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot