p>The successful candidate will have: • S. in Biology, Biochemistry, or related discipline with a minimum of 7+ years of experience, equivalent combinations of education and experience will be considered • Expertise with UPLC systems, Thermo (Chromeleon) preferred • Excellent communication skills with the proven ability to build open and collaborative relationships and successfully work as a member of a multidisciplinary team • Preferred Qualifications: • Expertise with nano and UPLC • Experience with UV/VIS, Fluorescence, CAD, quadrupole MS, ICP-MS detection • Experience with viral vectors (e.g., AAV, LVV) and/or additional analytical methods (dPCR, qPCR, ELISA, etc.) a plus • Self-motivated and organized • Ability to work in a fast-paced environment, meet deadlines, and prioritize work on multiple projects • 100% compliance with personal protective equipment (PPE) requirements in laboratory environments, including gloves, protective clothing, and eye safety glasses • Ability to perform physical tasks required for the role, including standing, walking, bending, kneeling, sitting, working your hands in a biosafety cabinet, and occasionally moving materials up to 50 pounds • Ability to work onsite 5 days/week at our Louisville, CO location.
• Develop and execute UPLC methods to quantify process reagents to demonstrate effective clearance • Collaborate with AD and QC team members on various stages of analytical method lifecycle (development/qualification/transfer) • Collaborate with systems engineer to create sample submission and result reporting workflow to support ongoing testing • Maintain clear records of experimental work using an electronic notebook system that adheres to company guidelines • Manage and prioritize sample submissions for respective method(s) and report data in timely manner • Prepare technical data reports and presentations • Contribute to other analytical method(s) development and testing as necessary • Exemplify the company core values and adhere to company policies to ensure safety and quality of gene therapy products and facility.