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:

The Opportunity

Bio-Techne Corporation (NASDAQ: TECH) is a global life sciences company providing innovative tools and bioactive reagents for the research and clinical diagnostic communities. Bio-Techne products assist scientific investigations into biological processes and the nature and progress of specific diseases. They aid in drug discovery efforts and provide the means for accurate clinical tests and diagnoses. Bio-Techne’s Diagnostics Division, which is comprised of the Asuragen and Exosome Diagnostics brands, develops molecular assays and software solutions that broaden access to care, answer unmet needs, and improve health outcomes through novel reagent systems and an industry-leading exosome enrichment technology for liquid biopsies.

Asuragen is a molecular diagnostic product company based in Austin, TX, changing the way patients are treated in genetics and oncology. Asuragen’s diagnostic systems, composed of proprietary chemistry and software, deliver powerful answers using broadly installed instrument platforms. They are simple to adopt and expand the ability to serve patients. Asuragen is a leading developer and manufacturer of cutting-edge molecular solutions (test kits, software, and controls) with a focus on oncology, inherited genetic disorders, infectious diseases and companion diagnostic products. With a global presence, we are committed to delivering high-quality solutions to researchers, healthcare professionals and laboratory diagnosticians worldwide.

The Operations department is seeking an Advanced Research Associate with experience running and troubleshooting molecular assays, preferably in a manufacturing environment. This role will support end to end production with primary focus on the formulation and quality control of reagents prior to being processed into finished kits.

What You’ll Do

· Follow manufacturing protocols to formulate reagents.

· Functionally test products, reviewing data obtained for compliance to established specifications.

· Propose solutions to technical issues with management or technical lead prior to executing.

· Assist in downstream production by following work instructions to fill, label and package reagents.

· Maintains quality of manufactured products; recording information accurately while following Good Documentation Practices as well as verifying work performed by co-workers.

· Document non-conformances and deviations.

· Follows work instructions to inspect, test and release raw materials.

· Perform rework as required according to designated work instructions.

· Coordinate and perform equipment maintenance.

· Perform equipment validation as required.

· Perform product stability testing according to work instructions.

· Maintain accurate inventory through the timely and accurate completion of work order and inventory transactions and by performing weekly cycle counts.

· Perform general lab maintenance, cleaning, and organization.

· Execute work in a safe manner. Notifying management of any safety issues or risks and assisting in remediation of those safety issues or risks.

· Apply experience and logic to resolve a variety of moderately complex problems.

· Provide support for cross-functional teams on complex projects.

· Identify and implement process improvements.

· Revise and update procedures as needed.

· Perform all other duties as assigned.

Who You Are & What You Bring

· Experienced in the setup and analysis of Molecular assays, PCR/CE, qPCR and NGS preferred.

· Skilled in the use of software programs such as Microsoft Office and database management programs.

· Organized, process-oriented individual with an attention to detail.

· Good time management skills.

· Ability to perform repetitive tasks with high degree of accuracy.

· Good written and communication skills.

· Able to work in a fast-paced environment.

· Readily adaptable to changing demands.

· Familiarity with ERP systems, QAD a plus.

· Ability to work cohesively in a team environment.

· Knowledge of lean manufacturing principals.

· Knowledge of cGMP, GLP, ISO, CE or other regulated environments.

Minimum Education and Experience Requirements

Bachelor’s degree in a scientific discipline or equivalent and 2-5+ years’ experience in a production environment; or a combination of education and applicable work experience.