Develop and optimize enzymatic detergents, high- and low-level disinfectants, and refurbishing chemistries for medical devices and healthcare surfaces. Design and execute laboratory studies to evaluate cleaning efficacy (protein, blood, biofilm removal), enzyme activity, antimicrobial efficacy, material compatibility, and stability. Select and evaluate raw materials including enzymes (protease, amylase, lipase), surfactants, oxidizers, quaternary ammonium compounds, peracetic acid systems, and corrosion inhibitors. Support disinfection validation testing (e.g., bactericidal, virucidal, fungicidal claims) in collaboration with internal teams or external labs. Partner with cross-functional teams (Regulatory, Quality, Clinical Affairs, Manufacturing) to ensure compliance with FDA, EPA, ISO 15883, AAMI, and other applicable standards. Assist in scale-up, technology transfer, and manufacturing troubleshooting for commercialization. Investigate and resolve product performance issues, including residue formation, material compatibility, and process variability. Maintain detailed documentation for formulations, validation data, technical reports, and regulatory submissions. Monitor industry trends in infection prevention, device reprocessing, and emerging antimicrobial technologies. Work in a laboratory and pilot-scale formulation development environment, interacting with manufacturing and sterile processing environments as needed. Handle bio-relevant soils, chemicals, and antimicrobial agents under strict safety protocols.
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Job Type
Full-time
Career Level
Mid Level