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Medical Device Reprocessing Jobs (NOW HIRING)

ICU Medical

Engineer II, Biocompatibility

$99K - $136K/yr

... medical device reprocessing procedures. * Contribute to the development and implementation of biocompatibility strategies (Experimental paradigm development). * Collaborate closely with external test ...

Medline

Sr. Director

Anaheim, CA

$177K - $266K/yr

Direct day-to-day manufacturing and production operations across a complex, high-SKU medical device reprocessing environment * Lead and develop supervisors, production leadership, and operations ...

HOYA Vision Care

Sr. Project Manager - R&D

Ramsey, MN · On-site

$100K/yr

... medical device reprocessing and disinfection solutions. In the information technology field, we provide products such as optical lenses, photomasks and blanks used in the manufacturing process for ...

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How much do medical device reprocessing jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for medical device reprocessing in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What is the salary for reprocessing techs?

The average salary for medical device reprocessing technicians typically ranges from $30,000 to $45,000 per year, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced techs with specialized skills can earn higher wages. Many facilities also offer benefits such as health insurance and paid time off.

Is becoming a sterile processing tech worth it?

Medical device reprocessing, or sterile processing technician, is a vital role in healthcare that involves cleaning, sterilizing, and maintaining surgical instruments. The job offers steady employment, requires attention to detail, and often involves certification such as CBSPD or IAHCSMM, with opportunities for advancement and good job stability.

What are the key skills and qualifications needed to thrive in the Medical Device Reprocessing position, and why are they important?

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 job?

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.

Where do sterile processing techs make the most money?

Sterile processing technicians tend to earn higher salaries in regions with a higher cost of living and greater healthcare demand, such as urban areas and states with robust healthcare systems. Salaries can also increase with experience, certifications, and working in larger hospitals or specialized medical facilities.

What skills are needed for reprocessing?

Medical device reprocessing requires attention to detail, knowledge of sterilization procedures, and adherence to safety protocols. Skills in operating cleaning and sterilization equipment, understanding infection control standards, and following strict guidelines are essential for ensuring devices are properly prepared for reuse.
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Medical Device Reprocessing jobs near you
Infographic showing various Medical Device Reprocessing job openings in the United States as of June 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 100% In-person job distribution, with an average salary of $76,384 per year, or $36.7 per hour.
Engineer II, Biocompatibility

Engineer II, Biocompatibility

ICU Medical

Remote

$99K - $136K/yr

Full-time

Posted 3 days ago

ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

165th of 516 rated manufacturers

Job description

Job Description
Position Summary
We are seeking a Biocompatibility Engineer II to join our team. As a member of the biocompatibility team, you will help ensure patient safety by contributing to the biological and toxicological evaluations of medical devices, materials, and processes. You will work closely with cross-functional teams to comply with global regulatory standards such as ISO 10993.
You will leverage your understanding of the medical device biocompatibility field to provide guidance throughout the product development cycle, interpret regulatory requirements, and support the biocompatibility strategy. Using your analytical skills, you will review scientific data, identify gaps, and recommend risk mitigation strategies.
This position will be pivotal in supporting regulatory compliance, quality engineering strategies, and design history file (DHF) remediation aligned with medical device regulations and standards such as EU MDR, FDA 510(k), ISO 13485, ISO 10993, ISO 18562, and ISO 14971.
Essential Duties & Responsibilities
  • Conduct biocompatibility assessments and evaluations in accordance with biological evaluation standards and regulatory requirements.
  • Collaborate with cross-functional teams to support multiple projects and meet schedules as defined by the larger project team.
  • Evaluate and reviews biocompatibility test data, protocols, and results.
  • Assist with regulatory submissions and address biological safety concerns in design meetings.
  • Stay informed of external standards and industry requirements for medical device biological safety, which is not limited to internal and external gap assessment evaluations for standards that govern both the biocompatibility and medical device reprocessing procedures.
  • Contribute to the development and implementation of biocompatibility strategies (Experimental paradigm development).
  • Collaborate closely with external test labs to ensure validity and appropriateness of test methodology, conduct, and reporting.
  • Write biological evaluation plans, reports, and other biocompatibility-related materials.
  • May participate in reviewing and improving policies, processes, and procedures pertinent to Biocompatibility Team.
  • Maintain positive, cooperative, and timely communication with all levels of employees, customers, contractors, and vendors.

Knowledge & Skills
  • Fundamental understanding of ISO 10993 standards, biomaterials, toxicological risk assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology.
  • Proficient in MS Office and excellent written and verbal communication skills.
  • Ability to work in a fast-paced, changing environment, prioritize tasks, and meet deadlines.
  • Communicate results, risks, and rationale with precision and in a timely manner to drive alignment on scope, expectations, and decisions, supporting on-time execution and adherence to project timelines while ensuring defensible biological safety conclusions.
  • Organized and detail-oriented with strong follow-up skills and experience in a cross-division business unit.

Minimum Qualifications, Education & Experience
  • Must be at least 18 years of age.
  • Bachelor's degree in chemical or biomedical engineering, or related field, from an accredited college or university is required.
  • 2+ years of Industry (Medical Devices) experience with a Bachelor.
  • A Master's Degree or PhD in a relevant field may substitute for industry experience.

Work Environment
  • This is largely a sedentary role.
  • This job operates in a professional office environment and routinely uses standard office equipment.
  • Typically requires travel less than 5% of the time

About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:
  • Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
  • The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
  • IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
  • Significant US IV solutions manufacturing and supply capabilities.

This role is based remotely; the incumbent may be remote in any state other than Colorado; California; Connecticut; Montana, Maine or New York.
ICU Medical EEO Statement:
ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
Know Your Rights: Workplace Discrimination is Illegal Poster
ICU Medical CCPA Notice to Job Applicants

What ICU Medical employees say

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About ICU Medical

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

San Clemente, CA, US

Year founded

1984

Social media

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