Advanced Research Associate - ProteinSimple QC

Posted 13 Days Ago
Be an Early Applicant
Minneapolis, MN, USA
In-Office
50K-82K Annually
Mid level
Biotech
The Role
The Advanced Research Associate is responsible for quality control testing, data management, and cross-functional collaboration to ensure product quality and compliance in the ProteinSimple lab.
Summary Generated by Built In

By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range:

$49,700.00 - $81,650.00

Position Summary: 

Perform routine quality control testing to determine lot status and product release for the ProteinSimple capillary electrophoresis basis systems, including iCE and SimpleWestern.  This position is responsible for planning, executing, and managing activities in the ProteinSimple liquid and lyophilized reagent QC process to ensure that all applicable objectives are met, and the product functions as expected. To be successful in this role candidate needs to be skilled in analytical techniques for analysis of biological assays. This position interfaces with Manufacturing, Process Engineering, Product Support, Assay Development and Quality Assurance. 

Key Responsibilities: 

  • Compile, document, interpret and manage data from ProteinSimple capillary electrophoresis systems, including iCE and Simple Western platforms, to evaluate the quality of in-process materials and finished goods to either confirm compliance with established quality standards or identify deviations. This includes functional, assay performance, precision, and accuracy testing. Data management comprises analysis and disposition of data produced and curation of that data into established systems. 

  • Ensure that the final product satisfies the product requirements and meet end-user expectations 

  • Revise SOPs of moderate complexity 

  • Initiate and support deviation and out-of-specification investigations 

  • Provide recommendations for corrective actions for low complexity problems and processes 

  • Spot areas for improvement to enhance the QC testing and process efficiency 

  • Maintain clear and accurate records 

  • Attend cross-functional team meeting and present data summaries 

  • Perform lab work when needed, including preparation of controls and reagents, and performing instrument runs 

  • Support projects and new product launch activities of moderate scope that require data review, and contribute to basic project deliverables 

  • May participate in method validations, establishing specifications and writing standard operating procedures 

  • Train team members within the department 

  • Support other QC operations, as needed 

Education and Experience: 

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

  • Master’s degree in Biology, Chemistry, Engineering, or similar relevant experience 

Knowledge, Skills and Abilities: 

  • 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 focused in algebraic equations for solving calculations 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 other tasks beyond daily expectations 

  • Flexibility to effectively prioritize own work and manage the work of multiple tasks 

  • Experience working with and evaluating data with Excel and proficient in all Microsoft Windows functions, as well as JMP and GraphPad Prism 

  • Ability to evaluate moderate volumes of data in a short timeframe 

  • Strong understanding of quality system regulations and standards 

  • Experience working within an ISO compliant, or other regulated environment. 

  • Experience developing, reviewing, deploying Standard Work (WI’s, MI’s, SOPs) 

  • Experience presenting assay data and interpretations 

  • Demonstrated ability to deliver quality work, with high work accuracy. 

  • Demonstrated ability to meet project timelines and collaborate with internal team 

  • Organized with exquisite attention to detail 

  • May be on computer monitor and keyboard for long periods of time

Why Join Bio-Techne:

  • We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
  • We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
  • We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. 
  • We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
  • We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

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.

To protect the interests of all, 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.

Bio-Techne Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Bio-Techne and has not been reviewed or approved by Bio-Techne.

  • Healthcare Strength Medical and dental coverage are often regarded as strong, with core health benefits broadly available across U.S. roles. Day-one eligibility and comprehensive options are described as a relative bright spot even when pay sentiment is mixed.
  • Leave & Time Off Breadth PTO, paid holidays, paid parental leave, and volunteer time are emphasized alongside flexible scheduling. Work-life balance elements are seen as strengths relative to base-pay concerns.
  • Strong & Reliable Incentives Quarterly or semi-annual bonuses and eligibility for annual cash incentives add meaningful upside for many salaried roles. Structured plans such as a Management Incentive Plan reinforce predictability of variable pay.

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The Company
HQ: Minneapolis, MN
2,512 Employees
Year Founded: 1981

What We Do

Bio-Techne Corporation (NASDAQ: TECH) is a leading developer and manufacturer of high-quality purified proteins and reagent solutions - notably cytokines and growth factors, antibodies, immunoassays, biologically active small molecule compounds, tissue culture reagents, and cell and gene therapy workflow solutions including T-Cell activation technologies. Bio-Techne’s portfolio also includes protein analysis solutions, sold under the ProteinSimple brand name, that offer researchers efficient and streamlined options for automated Western blot and multiplexed ELISA workflow. These reagent and protein analysis solutions are sold to biomedical researchers, as well as clinical research laboratories, and constitute the Protein Sciences Segment. Bio-Techne also develops and manufactures diagnostic products including FDA-regulated controls, calibrators, blood gas and clinical chemistry controls, and other reagents for OEM and clinical customers. Bio-Techne’s genomic tools include advanced tissue-based in situ hybridization assays (ISH) for research and clinical use, sold under the ACD brand, as well as a portfolio of clinical molecular diagnostic oncology assays including the ExoDx®Prostate (IntelliScore) test (EPI) for prostate cancer diagnosis. These diagnostic and genomic products comprise Bio-Techne’s Diagnostics and Genomics Segment. Bio-Techne products are integral components of scientific investigations into biological processes and molecular diagnostics, revealing the nature, diagnosis, etiology and progression of specific diseases. They aid in drug discovery efforts and provide the means for accurate clinical tests and diagnoses. With thousands of products in its portfolio, Bio-Techne generated approximately $714 million in net sales in fiscal 2019 and has over 2,200 employees worldwide.

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