Advanced Research Associate - ProteinSimple QC

Perform routine quality control testing to determine lot status and product release for the Protein Simple capillary electrophoresis basis systems, including iCE and Simple Western. This position is responsible for planning, executing, and managing activities in the Protein Simple liquid and lyophilized reagent QC process to ensure that all applicable objectives are met and the product functions as expected.

• Compile, document, interpret and manage data from Protein Simple capillary electrophoresis systems to evaluate the quality of in-process materials and finished goods.
• Perform functional, assay performance, precision, and accuracy testing; analyze data and disposition; curate into established systems.
• Ensure final product satisfies product requirements and meets end‑user expectations.
• Revise SOPs of moderate complexity; initiate and support deviation and out‑of-specification investigations.
• Recommend corrective actions; spot areas for improvement to enhance QC testing and process efficiency.
• Maintain clear, accurate records; attend cross‑functional team meetings and present data summaries.
• Perform lab work (prepare controls, reagents, run instruments) as needed.
• Support projects and new product launch activities of moderate scope; contribute to basic project deliverables.
• May participate in method validations, establish specifications, and write SOPs.
• Train department team members and support other QC operations as needed.

• Bachelor’s degree in Biology, Chemistry, Engineering or similar science degree with 2+ years’ experience.
• Master’s degree or relevant experience preferred.

• Knowledge of basic laboratory equipment and skills such as micropipetting, electrophoresis, isoelectric focusing, western blotting, QC functions, test procedures.
• Ability to apply understanding of electrophoresis techniques and data analysis to technical troubleshooting or project execution.
• Outstanding analytical skills, particularly in algebraic equations related to evaluating chromatograms.
• Ability to independently troubleshoot abnormal test results and determine next steps of moderate complexity.
• Work fully independently on routine tasks and beyond daily expectations.
• Flexibility to prioritize own work and manage multiple tasks.
• Experience evaluating data with Excel, proficient in Windows functions, JMP, Graph Pad Prism.
• Strong understanding of quality system regulations and standards, experience in ISO compliant or regulated environment.
• Experience developing, reviewing, deploying Standard Work (WIs, MIs, SOPs).
• Ability to present assay data and interpretations.
• Demonstrated ability to deliver quality work with high accuracy, meet project timelines and collaborate with internal team.
• Organized with exquisite attention to detail.
• May require extended computer use.

• Competitive insurance benefits starting on day one (medical, dental, vision, life, short‑term disability, long‑term disability, pet, legal and d).
• 401(k) plan, Employee Stock Purchase Plan (ESPP), Health Savings Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
• Mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs.
• Employee resource groups, volunteer paid time off, employee events and charity drives.
• Accrued leave policy with paid holidays, paid time off, and paid parental leave.

Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.