Research Associate, Analytical QC
Job in
Minneapolis, Hennepin County, Minnesota, 55400, USA
Listed on 2026-06-18
Listing for:
Research & Diagnostic Systems, Inc.
Full Time
position Listed on 2026-06-18
Job specializations:
-
Quality Assurance - QA/QC
-
Research/Development
Job Description & How to Apply Below
Overview
Bio-Techne offers a Research Associate, Analytical QC position focused on routine quality control testing of protein, peptide, or antibody products. Responsibilities include performing, documenting, and reporting QC data, maintaining instrumentation, and supporting lab operations.
Pay Range: $34,600 - $66,250 per year.
Key Responsibilities- Perform routine QC testing following SOPs, including concentration determination, SDS‑PAGE with densitometry, endotoxin assay, total organic carbon (TOC), conductivity, and other assigned tests.
- Document, analyze, and report QC results within the department and to cross‑functional groups.
- Calibrate and maintain laboratory instruments; order reagents and supplies; ensure waste disposal and laboratory cleanliness.
- Peer‑review laboratory documentation for accuracy and suggest improvements; collect and analyze QC metrics.
- Participate in laboratory meetings and provide suggestions to improve safety, efficiency, and effectiveness.
- Undertake additional duties as assigned and work toward departmental performance goals.
- B.S. degree in Biochemistry, Chemistry, Biology, or a related field.
- 0–2 years of related laboratory experience.
- Strong attention to detail, organization, data analysis, and problem‑solving skills.
- Ability to work in a fast‑paced environment, multitask, and communicate effectively, both verbally and in writing.
- Knowledge of biochemistry as applied to protein, peptide, and antibody products; basic laboratory equipment and QC functions.
- Understanding of standard operating procedures, aseptic technique, and safety regulations.
- Proficiency with Microsoft Word, Excel, and web browsers; entry and typing skills.
- Critical thinking, decision‑making, and execution of appropriate actions within SOPs.
- Technical writing and clear verbal communication.
- Discretion with sensitive and proprietary information.
- High accuracy and independent work on routine assignments and team projects.
- Ability to work standard business hours (8:00AM–5:00PM) with flexibility for additional hours as needed.
- Competitive insurance benefits starting 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, Health Savings Account, and Flexible Spending Accounts.
- Learning and development, tuition reimbursement, mentorship, promotion opportunities, internship programs.
- Employee resource groups, volunteer paid time off, events, and charity drives.
- Accrued leave policy with paid holidays, PTO, and paid parental leave.
- Culture of empowerment, innovation, and inclusion.
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. For assistance with accommodations, contact
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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