Microbiologist

Colorado Chromatography Labs is a cutting‑edge life science organization and operating company of Sunflower Wellness, with over 50 years of collective expertise in synthetic chemistry, formulations, analytical and biological testing. We specialize in developing safe, scalable, and cost‑effective natural product solutions: from analytical method development and in vitro bioassays to oncology research and novel molecule discovery. Our team actively collaborates with academic institutions and contributes published research and patented innovations that advance therapeutic discovery across disease areas. We foster a lab culture built on safety, precision, curiosity, and ethical research. With a collaborative team where your work moves from concept to real‑world impact, and opportunities to grow across disciplines within both CCL and the broader Sunflower Wellness ecosystem, this is science with purpose. Join our team and grow with a company that’s shaping the future of life sciences. Role Summary The Microbiologist supports the analytical testing operations of a new peptide testing venture, with a primary focus on bacterial endotoxin and sterility testing for peptide products. This role operates within a rigorous quality management environment as the laboratory builds toward ISO/IEC 17025 accreditation, and requires expertise in USP compendial methods and aseptic technique. Success in this role means accurate, defensible test results delivered on time with full documentation integrity. Responsibilities Perform bacterial endotoxin testing of peptides using LAL and/or recombinant Factor C (rFC) methods per USP and/or . Perform sterility testing by the compendial method per USP (Valiteq ExtenDATE), and/or by a validated rapid alternative method (e.g., BacT/ALERT) per USP . Prepare samples, standard endotoxin curves, and controls; calculate endotoxin limits and maximum valid dilution; interpret and report results. Conduct method suitability testing for each peptide product, including interference screening for the endotoxin method and bacteriostasis/fungistasis testing for sterility. Maintain aseptic technique and ISO‑classified clean‑area conditions during all sterility testing activities. Operate, calibrate, and maintain plate reader and related laboratory equipment. Document all testing per the laboratory's quality management system and data‑integrity requirements, aligned with ISO/IEC 17025 as the lab works toward accreditation; record results in LIMS and issue test reports. Recognize and report out‑of‑specification or nonconforming results, and suppor investigations under supervision. Qualifications Bachelor’s degree in Microbiology, Biology, Biochemistry, or a related life sciences field. Valid driver’s license. Hands‑on experience performing bacterial endotoxin testing using LAL and/or recombinant Factor C (rFC) methods. Hands‑on experience performing sterility testing using Valiteq ExtenDATE and/or by a validated rapid alternative method. Working knowledge of USP , , , and , in addition to aseptic technique in ISO‑classified clean areas. Familiarity with ISO/IEC 17025 quality management and documentation practices. Attention to detail and ability to work both independently and as part of a team. #J-18808-Ljbffr