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Senior Research Associate - ProteinSimple QC

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: Research & Diagnostic Systems, Inc.
Per diem position
Listed on 2026-06-18
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 62300 USD Yearly USD 62300.00 YEAR
Job Description & How to Apply Below

Position Summary

Perform routine quality control testing to determine lot status and product release for the Protein Simple capillary electrophoresis based 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. The role requires strong analytical skills and experience with biological assays and interfaces with manufacturing, process engineering, product support, assay development, and quality assurance.

Pay Range: $62,300.00 - $.

Key Responsibilities
  • Compile, document, interpret, and manage data from Protein Simple capillary electrophoresis systems to evaluate the quality of in-process materials and finished goods, confirming compliance with established quality standards or identifying deviations.
  • Perform functional, assay performance, precision, and accuracy testing and manage data analysis, disposition, and curation into established systems.
  • Ensure that the final product satisfies product requirements and meets end‑user expectations.
  • Initiate and support deviation and out‑of‑specification investigations and recommend corrective actions.
  • Spot areas for improvement to enhance QC testing and process efficiency.
  • Maintain clear and accurate records and attend cross‑functional team meetings presenting data summaries.
  • Perform lab work when needed, including preparation of controls and reagents and instrument runs.
  • Support projects and new product launch activities, providing data review of unclear factors and basic project deliverables.
  • Responsible for new method validations, establishing specifications, and writing standard operating procedures.
  • Train and provide scientific guidance to others as needed.
  • Provide support to other QC operations when required.
Education and Experience

Bachelor’s degree in Biology, Chemistry, Engineering or a related science field plus 5+ years of experience;
or Master’s degree in the same areas with 3+ years of experience.

Knowledge,

Skills and Abilities
  • Knowledge of basic laboratory equipment and skills such as micropipetting, QC functions, test procedures, and aseptic technique.
  • Understanding of electrophoresis techniques and data analysis for troubleshooting or project execution.
  • Proficiency in R analysis (a plus).
  • Ability to work independently on routine and complex tasks, and to prioritize multiple assignments.
  • Super user level in Excel and proficiency in all Microsoft Windows functions.
  • Strong data evaluation skills in a short timeframe and a strong presentation skill set.
  • Experience with ISO‑compliant or other regulated environments and developing, reviewing, and deploying SOPs and other standard works.
  • Experience with immunoassay methodology (a plus).
  • Outstanding analytical skills and a track record of delivering quality work with high accuracy.
  • Demonstrated ability to meet project timelines and collaborate with internal teams while maintaining exquisite attention to detail.
Benefits
  • Competitive insurance benefits starting on day one: medical, dental, vision, life, short‑term and long‑term disability, pet, legal and d.
  • 401(k) plan with company match, employee stock purchase plan, HSA, FSA, and Dependent Care FSA.
  • Career development through mentorship, promotion opportunities, training and development, tuition reimbursement and 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.
EEO Statement

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.

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Position Requirements
10+ Years work experience
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