Entry Level, Junior
Pay Range: $25.60 - $35.20
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment.
Prepare products using approved procedures and keep detailed and accurate records
Perform in process analysis and determine adjustments to bring analytes into specification
Analyze products, stock solutions, and raw materials using automated and manual instrumentation
Evaluate that the analysis instrumentation and procedure is operating correctly, and verify or perform maintenance before use
Measure accurately quantities of material volumetrically and gravimetrically, employing knowledge of chemical and biochemical properties and handling procedures
Continually evaluate and/or create work instructions, QCRs, SOPs and other documents and procedures for effectiveness and modify through formal change process
Perform processing steps as required in the documentation such as centrifugation, diafiltration, in-process filtration, and column separation
Perform final release testing
Perform aseptic procedures such as aliquoting, filtration, and microbial plating
Perform assay testing for Value Assignment as required
Assist in developing ways to increase efficiency and/or reduce costs
Assist with overall maintenance and cleanliness of the laboratory and equipment
Strong attention to detail, maintain clear detailed and accurate records
Perform additional functions as required
Ability to show initiative and to perform in a multi-task environment
Good interpersonal and verbal/written communication skills.
Ability to work with personnel of all levels
Ability to perform in a GMP and GLP environment. Knowledge of QSR and ISO
Familiarity with biohazardous material handling and chemical safety procedures
Bachelor’s degree in Chemistry, Biochemistry, Biological Science, or related field preferred with 0-2 years work experience in In Vitro diagnostics, medical device, pharmaceutical or related industry required.
*This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status). If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact hr@bio-techne.com for assistance. *
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