Bio-Techne • Minneapolis, MN 55405
Job #2670099380
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:
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne's evolving portfolio.
Key Responsibilities:
Perform technical processing steps as required in the documentation, including Luminex Multiplex Assays, ELISA Assays, and Simple Plex Assays
Set up and conduct your own experiments to manufacture new batches of product
Draft and revise standard operating procedures
Analyze in-process assay data and determine adjustments to bring analytes into specification
Measure quantities of material volumetrically and gravimetrically, with accuracy, employing knowledge of chemical and biochemical properties and handling procedures
Analyze products, stock solutions, and raw materials using automated and manual instrumentation
Assist in the validation testing of equipment and processes
Perform final release testing and confirm materials are passing specification
Document results and complete reporting for manufacturing batches
Assist in harmonizing new materials with components from other departments for a functional assay batch
Carry out troubleshooting activities daily
Propose and implement process improvements
Collaborate with other departments and labs as needed
Help train new employees as needed
Follow company policies and practices as outlined in the Handbook
Follow guidelines and comply with all company safety, quality, and training procedures and regulations
Perform additional duties as assigned
Qualifications
Education and Experience:
Bachelor's degree and 2-4 years of relevant experience
Or, Master's degree in a related field and up to 2 years of relevant experience
Knowledge, Skills, and Abilities:
Working knowledge of Microsoft Word and Excel is required
Must be able to work in a fast-faced environment where you will be required to prioritize your own work to meet various deadlines
Must be able to analyze data to make effective decisions
Must have good verbal and written communication skills, especially across different groups
Must have strong organizational skills and attention to detail
Must work well independently in an environment that requires strategic decision making
Must demonstrate strong technical knowledge
Ability to perform in a GMP and GLP environment. Knowledge of QSR and ISO
Familiarity with biohazardous material handling and chemical safety procedures
Why Join Bio-Techne:
We offer competitive salaries along with extensive medical, vision, and dental plans for you and your family starting on day one!
We invest in our employees' financial futures through 401k matching and an employee stock purchase plan.
We help our employees develop their careers through mentorship, promotional opportunities, training and development, internship programs, and more.
We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.
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 is an E-Verify Employer in the United States.
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