Senior Manufacturing Associate I/II (Days)

Senior Manufacturing Associate I/II performs upstream and/or downstream biopharmaceutical manufacturing in a GMP/GLP environment, following approved procedures and Right First Time principles. Responsibilities include manufacturing bulk intermediates and drug substances per batch records, operating in a cleanroom with aseptic controls, documenting manufacturing records and logbooks, maintaining equipment per SOP, ensuring material issuance and accounting (SPR, BPR and Forms), applying GDP/good manufacturing principles, contributing to 5S workplace organization, providing guidance to Manufacturing Associates, and supporting supervisory workload distribution. Qualifications involve a Bachelor's degree (or equivalent experience) with 4-6 years (I) or 5+ years (II) of GMP manufacturing operations or a high school diploma with extensive experience. The role offers salary ranges by level, plus benefits (bonus, medical/dental/vision, PTO/holidays, 401K with vesting), and is with KBI Biopharma, a global CDMO. Shift: 6:00 AM – 6:30 PM, 2-2-3 schedule, Boulder, CO location.