QC Apps Specialist: Data Automation & Validation

Abbott; Alabama; On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott in Madison, WI is hiring a QC Applications Specialist to lead and participate in quality control automation and data analysis. You will manage EFD forms, data trending, QC analysis workbooks, and validation efforts under cGMP/GLP guidelines.

The role requires a life sciences degree with 4+ years biotech experience or an advanced degree with 2+ years, plus SAS JMP and scripting skills. Some travel and cross-functional collaboration are expected.

Qualifications

• Bachelor’s degree in Analytical or Life Sciences required with 4+ years biotech experience, or advanced degree with 2+ years.
• 1+ years of SAS JMP or similar software for data trending and evaluation.
• 1+ years coding & scripting in software/statistical apps.
• 2+ years in GMP/ISO13485 lab environment with strong documentation.

Responsibilities

• Lead or support QC Applications and Automation projects.
• Develop/validate QC analysis workbooks for data evaluation.
• Create/write quality docs per cGMP/GLP guidelines.
• Mentor team members on QC applications and automation.
• Assist CAPA and deviation reporting.
• Travel up to 10% between Madison locations and up to 5% out of town.

Skills

SAS JMP

Data trending

Coding/scripting

GMP/ISO knowledge

Excel

MS Office

JSL (preferred)

Team mentoring

Education

Bachelor's degree in Life Sciences

Master's degree or PhD in Life Sciences/MATH

Tools

SAS JMP

Excel

Job description

Abbott in Madison, WI is hiring a QC Applications Specialist to lead and participate in quality control automation and data analysis. You will manage EFD forms, data trending, QC analysis workbooks, and validation efforts under cGMP/GLP guidelines.

The role requires a life sciences degree with 4+ years biotech experience or an advanced degree with 2+ years, plus SAS JMP and scripting skills. Some travel and cross-functional collaboration are expected.