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Medical Device Reprocessing Jobs in New York (NOW HIRING)

Chemist

Jamaica, NY ยท On-site

... medical devices and healthcare surfaces * Design and execute laboratory studies to evaluate ... Monitor industry trends in infection prevention, device reprocessing, and emerging antimicrobial ...

Sr. Product Manager

Wayne, NJ ยท On-site

$125K - $165K/yr

Minimum 7+ years of experience in medical device, pharmaceutical, or life sciences product ... sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the ...

Sr. Product Manager

Wayne, NJ ยท Hybrid

$125K - $165K/yr

Minimum 7+ years of experience in medical device, pharmaceutical, or life sciences product ... sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the ...

Sr. Product Manager

Wayne, NJ ยท On-site

$124K - $164K/yr

Minimum 7+ years of experience in medical device, pharmaceutical, or life sciences product ... sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the ...

Product Assembler I

Wayne, NJ ยท On-site

$20/hr

Minimum experience is 0-12 months in a medical device-manufacturing environment. Required Knowledge ... sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the ...

Product Assembler I

Wayne, NJ ยท On-site

$20/hr

Minimum experience is 0-12 months in a medical device-manufacturing environment. Required Knowledge ... sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the ...

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Showing results 1-20

Medical Device Reprocessing information

See New York salary details

$23

$40

$77

How much do medical device reprocessing jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for medical device reprocessing in New York is $40.18, according to ZipRecruiter salary data. Most workers in this role earn between $27.07 and $50.24 per hour, depending on experience, location, and employer.

What does a medical device reprocessing tech do?

A medical device reprocessing technician is responsible for cleaning, disinfecting, sterilizing, and preparing medical instruments and devices for reuse in healthcare settings. They follow strict protocols, use specialized equipment, and often require certification to ensure patient safety and compliance with industry standards.

What are the key skills and qualifications needed to thrive in medical device reprocessing?

To thrive in Medical Device Reprocessing, you need attention to detail, manual dexterity, and a solid understanding of infection control principles, often supported by completion of a medical device reprocessing technician program. Familiarity with sterilization equipment, tracking systems, and knowledge of regulatory standards (such as CSA or AAMI certification) is typically required. Strong organizational skills, teamwork, and the ability to communicate clearly are valued soft skills in this field. These abilities ensure that medical devices are cleaned, sterilized, and ready for safe use, which is critical for patient safety and efficient healthcare operations.

What are the typical daily responsibilities of someone working in medical device reprocessing?

Medical Device Reprocessing professionals are responsible for cleaning, disinfecting, inspecting, assembling, and sterilizing surgical instruments and medical equipment. Daily tasks include carefully following protocols, operating sterilization machinery, documenting processes, and maintaining inventory of reusable instruments. This role often involves close collaboration with surgical teams and nursing staff to ensure that all equipment is prepared and delivered on time to support patient care. Working in this department typically requires strong attention to detail and the ability to meet deadlines in a busy, regulated healthcare environment.

What is a medical device reprocessing?

A Medical Device Reprocessing job involves cleaning, disinfecting, sterilizing, and inspecting medical instruments to ensure they are safe for patient use. Professionals in this field follow strict infection control guidelines and operate specialized equipment to maintain the integrity of reusable medical devices. They work in hospitals, clinics, and other healthcare settings, playing a crucial role in preventing infections and ensuring patient safety. This job requires attention to detail, knowledge of sterilization techniques, and adherence to healthcare regulations. Many employers require certification in medical device reprocessing or sterile processing.

How do you become a medical device reprocessing technician?

To become a medical device reprocessing technician, individuals typically need a high school diploma or equivalent and must complete on-the-job training or a certification program in medical equipment sterilization and reprocessing. Some employers prefer candidates with knowledge of infection control procedures and familiarity with sterilization tools and techniques.
Infographic showing various Medical Device Reprocessing job openings in New York as of August 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $83,567 per year, or $40.2 per hour.

Other

Re-posted 24 days ago


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.

ย 

What You Need to Succeed in This Position

  • Bachelorโ€™s degree in Chemistry, Biochemistry, Chemical Engineering, or related field
  • 3โ€“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