Quality Control Research Associate — Protein Analysis Systems

Bio-Techne; Minneapolis (MN); On-site; USD 40,000 - 66,000; Full time

Benefits offered by this job

Health insurance

401k and ESPP

HSA and FSA

Mentorship and development

Paid time off and holidays

Job summary

Bio-Techne is seeking a QC-focused analyst to perform routine quality control testing and manage reagent QC processes. You will ensure lot status alignment with product release and interface with Manufacturing, Process Engineering, Product Support, and QA to meet objectives.

The role requires laboratory capabilities in analytical techniques, data analysis, and meticulous documentation, with a strong emphasis on safety and quality standards. Knowledge of GMP practices is preferred.

Qualifications

• Bachelor’s degree in Biology, Chemistry, Engineering or similar science degree with 0-2 years of laboratory experience.
• Associates degree or non-scientific bachelor’s with 2+ years’ relevant experience in a GMP or life science quality position.

Responsibilities

• Run QC assays for reagents and consumables, analyze results, and review trending data.
• Record lot numbers, expiration dates, and observations meticulously.
• Revise SOPs of low complexity.
• Initiate deviation and out-of-specification investigations.
• Maintain inventory of reagents and consumables.
• Follow lab safety, quality, and training procedures.
• Participate in continuous process improvements.

Skills

Pipetting

Electrophoresis

Isoelectric focusing

Western blotting

Data analysis

Independent work

Organization

Time management

Statistical principles

Team support

Education

Bachelor’s degree in Biology, Chemistry, Engineering or similar science degree

Associates degree or non-scientific bachelor’s with 2+ years’ GMP/life science experience

Tools

MS Word

MS PowerPoint

MS Outlook

JMP

GraphPad Prism

Job description

Bio-Techne is seeking a QC-focused analyst to perform routine quality control testing and manage reagent QC processes. You will ensure lot status alignment with product release and interface with Manufacturing, Process Engineering, Product Support, and QA to meet objectives.

The role requires laboratory capabilities in analytical techniques, data analysis, and meticulous documentation, with a strong emphasis on safety and quality standards. Knowledge of GMP practices is preferred.