QC Applications Specialist

Abbott · Madison

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QualityFull-time$61k–$123kCompany career page

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Role summary

Abbott seeks a QC Applications Specialist in Madison to manage quality control automation, electronic databases, and statistical analysis systems. The role involves implementing and validating QC processes, developing analysis workbooks, and leading cross-functional quality initiatives in a regulated laboratory environment.

What they're looking for

Bachelor's degree in Analytical/Applied Chemistry, Molecular Biology, Biochemistry, or related field plus 4+ years biotechnology experience
1+ years SAS JMP or equivalent statistical software for data trending and evaluation
1+ years coding and scripting within software and statistical applications
2+ years GMP/ISO13485 laboratory experience with strong GMP documentation skills
Proficiency with Microsoft Office and Excel
Authorization to work in United States without sponsorship

What you'll be doing

Support Electronic Form Database processes, form development, and serve as subject matter expert for test method EFD forms
Lead or support quality control automation and liquid handling method script projects, including creation and implementation
Develop, validate, and improve QC analysis workbooks using SAS JMP or similar statistical software
Draft and execute validation protocols for quality system software in accordance with cGMP, FDA, and ICH guidelines
Write, update, and review quality documents including SOPs and test methods compliant with regulatory guidelines

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