Description

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.

Position Summary
In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques such as cell culture, flow cytometry, qPCR, and other analytical methods. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction.

Key Responsibilities

1. Lead method validation and instrument qualification projects that are small in scope/scale, with supervision
2. Assist with method/instrument validation projects
3. Create and review Standard Operation Procedures (SOP) and other Quality Management Systems related documents for the department
4. Generate technical method validation plans and reports
5. Assist with transferring new quality control testing methods from development to routine QC groups
6. With experience, train team members within department
7. Organize and coordinate communication between teams to drive projects forward
8. Follow company policies and practices as outlined in the handbook and follow guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job
9. Perform additional duties as assigned

Qualifications

Education and Experience

• 4-year science degree with a minimum of 2 years relevant industry experience or
• Master’s degree with minimal experience
• Experience within a quality-based role is preferred

Knowledge, Skills, and Abilities

• Experience with Good Manufacturing Practice (GMP) documentation and familiarity working under a quality management system (QMS) are required
• Attention to detail and a commitment to continuous improvement are required
• Technical writing skills are essential
• Experience in at least one of the following fields: cell culture, flow cytometry, molecular biology
• Able to perform basic statistical analyses
• Demonstrate adaptability by prioritizing projects as needed
• Willingness to learn new laboratory techniques and perform routine QC tests
• Ability to work hours that adhere to standard business operation (8:00 A.M to 5:00 P.M.)
• Flexibility to work alternate or additional hours as needed