Specialist, QA

📋 Description

• Primary duties and responsibilities of the position are as follows. Other duties may be assigned.
• 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.

🎯 Requirements

• Bachelor’s Degree or above in Chemistry or related Science AbbVie
• 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

🎁 Benefits

• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving
• US & Puerto Rico only - to learn more, visit the Equal Employment Opportunity employer page.