Research Associate - Analytical QC

5w1 month ago

Bio-Techne

Minneapolis, US · Full-time · $50,000 – $65,000

About this role

The Research Associate, Analytical QC will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. This role is crucial for enabling cutting-edge research in Life Sciences and Clinical Diagnostics.

Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, TOC, conductivity and other testing as assigned. The position requires routine documentation, analysis and communication of results within the department and across different groups. Additional duties involve instrument calibration, maintenance, record keeping, and lab support.

The Research Associate must pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Peer review of laboratory documentation and participation in laboratory meetings are also key aspects of the role. Interaction with group members is encouraged to improve safety and efficiency.

By joining Bio-Techne, you join a company with a powerful and positive purpose of enabling cutting-edge research. The role offers the chance to contribute to tools that further treat and prevent disease worldwide while developing skills in quality control and analytical methods. Opportunities for innovation and efficiency improvements are embedded in annual goal-setting.

Requirements

B.S. degree in Biochemistry, Chemistry, Biology, or a related field with 0–2 years related experience.
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 and its application to protein, peptide, and antibody products.
Knowledge of basic laboratory equipment, QC functions, test procedures, and aseptic technique.
Skills in problem solving and critical thinking, including the ability to make effective decisions within defined SOPs.
Skills in verbal and written communication, including technical writing skills.
Ability to pay attention to details and perform at a high level of accuracy.

Responsibilities

Perform, document, and report data for routine QC testing following standard operating procedures.
Assist with lab support functions including instrument calibration and maintenance, reagent ordering and preparation, waste disposal, and laboratory cleaning.
Assist with the monitoring of lab supplies and ordering.
Perform peer review of laboratory documentation to ensure accuracy and suggest improvements, and assist in the collection of metrics.
Participate in laboratory meetings and actively interact with group members to learn and provide suggestions for a safer, more efficient environment.
Follow company policies and practices as outlined in the Handbook and follow safety guidelines per AWAIR, Chemical Hygiene, and Exposure Control manuals.
Perform additional duties as assigned.

Benefits

Join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics.
Opportunity to pursue annual goals that facilitate innovation, efficiency, and team building across the QC Department or the entire company.
Work with a team that provides tools for researchers to further treat and prevent disease worldwide.