
Research Associate - GMP Process Development
6d6 days agoBio-Techne
Minneapolis, US · Full-time · $50,000 – $65,000
About this role
Bio-Techne is seeking a highly motivated and creative Research Associate to join our GMP Process Development team in Minneapolis. In this role, you will participate in the development, optimization, and technology transfer of protein purification procedures for recombinant proteins expressed in E. coli cell lines to our GMP production facility.
Your day-to-day work will involve setting up and conducting experiments that further new product development, following standard operating procedures, and documenting results to prepare reports summarizing your data. You will also write protocols for the purification of recombinant proteins and assist with writing Design Control documents within the Quality Management System.
You will collaborate with other departments and labs as needed, working in a collaborative laboratory environment focused on high-quality recombinant protein products. The team is responsible for developing Bio-Techne's various product lines, with a focus on enabling cutting-edge research in Life Sciences and Clinical Diagnostics.
This is a great opportunity to work with cutting-edge biotech development and manufacturing processes while contributing to tools that help researchers further treat and prevent disease worldwide. You will be responsible for transferring and scaling developed procedures to support the company's powerful and positive purpose.
Requirements
- Bachelor's degree in Biological Sciences or equivalent
- 0-2 years of relevant experience in a laboratory setting
- Experience with protein purification procedures for recombinant proteins
- Familiarity with E. coli cell lines and expression systems
- Ability to follow standard operating procedures and safety guidelines
- Experience documenting experimental results and preparing technical reports
- Knowledge of GMP production facility practices and quality management systems
Responsibilities
- Support development of Bio-Techne reagents and consumables
- Set up and conduct experiments that further new product development
- Follow standard operating procedures
- Document results and prepare reports summarizing your data
- Responsible for transferring and scaling developed procedures
- Write protocols for the purification of recombinant proteins
- Collaborate with other departments and labs as needed
- Assist with writing Design Control documents within the Quality Management System
Benefits
- Opportunity to work with cutting-edge biotech development and manufacturing processes
- Collaborative laboratory environment focused on high-quality recombinant protein products
- Contribute to tools that enable research in Life Sciences and Clinical Diagnostics
- Work for a company with a powerful and positive purpose of enabling cutting-edge research
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