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Job Description
In This Position, You Will Have the Opportunity To
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.
What You Need to Succeed in This Position
Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or related field
3–6 years of experience in formulation development, preferably in medical, healthcare, or regulated cleaning products
Working knowledge of:
Enzyme-based cleaning systems and stability considerations
Surfactant systems and soil removal mechanisms (proteins, lipids, polysaccharides)
Disinfectant chemistries (e.g., oxidizing agents, aldehydes, quats)
Experience designing experiments and interpreting performance data
Strong understanding of laboratory safety and chemical handling practices
Technical depth in cleaning, enzymatic, and antimicrobial chemistry
Familiarity with antimicrobial efficacy standards (e.g., AOAC, ASTM, EN methods), preferred
Knowledge of regulatory frameworks (FDA 21 CFR, EPA FIFRA, EU MDR, REACH), preferred
Product performance testing using ultrasonic machines and automatic washers with TOSI plates and challenge substrates, preferred
Accelerated shelf life and stability studies using an incubator, preferred
Strong analytical and problem-solving skills
Ability to translate laboratory results into practical application performance
Cross-functional collaboration in regulated environments
Attention to detail and documentation rigor
Project management and time prioritization
