Collaborate with Manufacturing, Quality, Engineering, Regulatory, and R&D teams to support ... Biomedical Sciences). * Entry-level candidates are acceptable. Required Skills & Qualifications
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Collaborate with Manufacturing, Quality, Engineering, Regulatory, and R&D teams to support ... Biomedical Sciences). * Entry-level candidates are acceptable. Required Skills & Qualifications
Team with Joint Replacement sales force and clinical specialist to achieve business goals. What you will need * Bachelor's degree in Biomedical Engineering, Surgical Instrumentation, Nursing, or a ...
Team with Joint Replacement sales force and clinical specialist to achieve business goals. What you will need * Bachelor's degree in Biomedical Engineering, Surgical Instrumentation, Nursing, or a ...
Team with Joint Replacement sales force and clinical specialist to achieve business goals. What you will need * Bachelor's degree in Biomedical Engineering, Surgical Instrumentation, Nursing, or a ...
Team with Joint Replacement sales force and clinical specialist to achieve business goals. What you will need * Bachelor's degree in Biomedical Engineering, Surgical Instrumentation, Nursing, or a ...
Technical Service Specialist
$45K - $89.80K/yr
As the Technical Service Specialist provides independent clinical and technical support in response ... Bachelor's Degree ( 16 years) preferably Electronic/Biomedical/Biology/Engineering or related field.
New
Technical Service Specialist
$45K - $89.80K/yr
As the Technical Service Specialist provides independent clinical and technical support in response ... Bachelor's Degree ( 16 years) preferably Electronic/Biomedical/Biology/Engineering or related field.
New
Entry Level Biomedical Clinical Engineer information
What are the key skills and qualifications needed to thrive as an Entry Level Biomedical Clinical Engineer, and why are they important?
To thrive as an Entry Level Biomedical Clinical Engineer, you need a solid background in biomedical engineering or a related field, with knowledge of anatomy, physiology, and medical device regulations. Familiarity with diagnostic and therapeutic equipment, equipment management software, and relevant safety certifications such as CBET is often expected. Strong analytical thinking, effective communication, and problem-solving abilities set candidates apart when interacting with medical staff and troubleshooting equipment issues. These skills ensure safe, efficient, and compliant operation of medical devices, directly impacting patient care quality.
What are some typical projects or responsibilities for an entry level biomedical clinical engineer during their first year?
As an entry level biomedical clinical engineer, you can expect to be involved in maintaining and troubleshooting medical equipment, conducting preventive maintenance, and supporting equipment inventory management. You'll likely work closely with clinical staff to ensure equipment is safe and operational, assist with equipment installations, and document compliance with regulatory standards. Early in your role, you'll also have opportunities to shadow senior engineers, participate in training sessions, and gradually take on more complex technical tasks as you build experience.
What does an Entry Level Biomedical Clinical Engineer do?
An Entry Level Biomedical Clinical Engineer is responsible for installing, maintaining, and repairing medical equipment in healthcare settings. They work closely with medical staff to ensure that devices like ventilators, monitors, and imaging equipment function safely and effectively. Other duties may include performing safety checks, troubleshooting technical problems, and assisting with equipment upgrades or replacements. This role is crucial for ensuring optimal patient care and compliance with regulatory standards.
What is the difference between Entry Level Biomedical Clinical Engineer vs Biomedical Equipment Technician?
| Aspect | Entry Level Biomedical Clinical Engineer | Biomedical Equipment Technician |
|---|---|---|
| Credentials | Bachelor's degree in biomedical engineering or related field; certifications like CBET (Certified Biomedical Equipment Technician) are common | Associate's degree or technical certification; CBET certification often preferred |
| Work Environment | Hospitals, clinics, healthcare facilities; involved in equipment management, troubleshooting, and clinical support | Medical equipment repair and maintenance in hospitals, clinics, or service centers |
| Employer & Industry Usage | Healthcare providers, medical device companies, biomedical service firms | Hospitals, medical device manufacturers, biomedical service companies |
While both roles involve working with medical equipment, Entry Level Biomedical Clinical Engineers focus on clinical support, troubleshooting, and equipment management with a biomedical engineering background. Biomedical Equipment Technicians primarily handle repair and maintenance tasks, often with technical certifications. Both roles are essential in healthcare settings but differ in scope and responsibilities.
What are the most commonly searched types of Biomedical Clinical Engineer jobs in Puerto Rico? The most popular types of Biomedical Clinical Engineer jobs in Puerto Rico are:
What are popular job titles related to Entry Level Biomedical Clinical Engineer jobs in Puerto Rico? For Entry Level Biomedical Clinical Engineer jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Entry Level Biomedical Clinical Engineer jobs in Puerto Rico look for? The top searched job categories for Entry Level Biomedical Clinical Engineer jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Entry Level Biomedical Clinical Engineer jobs? Cities in Puerto Rico with the most Entry Level Biomedical Clinical Engineer job openings:
Full-time
Posted 14 days ago
Job description
Main Responsibilities:
- Support EO sterilization and microbiological testing activities within a regulated manufacturing environment.
- Perform microbiological analyses on raw materials, in-process materials, release samples, and stability samples.
- Prepare, clean, disinfect, sterilize, store, and handle laboratory instruments, materials, products, and supplies.
- Support sterilization validations including protocol execution, documentation, and report preparation.
- Interpret and evaluate analytical results against established specifications and support corrective action activities when necessary.
- Assist in developing, validating, and implementing controlled environment methods and laboratory procedures.
- Perform qualitative and quantitative testing using standard laboratory equipment and automated instrumentation.
- Support methodology transfer activities from R&D into manufacturing or laboratory operations.
- Maintain accurate technical documentation, validation records, protocols, and reports in compliance with GDP requirements.
- Collaborate with Manufacturing, Quality, Engineering, Regulatory, and R&D teams to support sterilization and microbiological initiatives.
- Participate in continuous improvement activities related to sterilization, laboratory operations, and microbiological processes.
- Follow FDA regulations, ISO standards, and company quality procedures.
- Minimum 3 year of relevant experience in the regulated industry.
- Bachelor’s degree in Science (Microbiology, Biology, Biotechnology, Biomedical Sciences).
- Entry-level candidates are acceptable.
- Knowledge of EO sterilization processes.
- Familiarity with FDA regulations, ISO 11135, ISO 11737, and related sterilization and microbiological standards.
- Strong technical documentation and report-writing skills.
- Ability to support sterilization validations, protocols, and testing activities.
- Strong analytical and problem-solving skills.
- Ability to communicate findings clearly and collaborate effectively with cross-functional teams including Manufacturing, Quality, Regulatory, and R&D.
- Fully bilingual (English and Spanish).
- Experience in regulated manufacturing, pharmaceutical, biotechnology, or medical device industries.
- Experience with TrackWise or similar quality management systems.
- Knowledge of environmental monitoring and controlled environments.
- Exposure to validation and laboratory quality systems.
- Microsoft Office Suite
- TrackWise
- Agile environment exposure
- Technical documentation
- Sterilization validation support
- Microbiological testing techniques
- Controlled environment practices
- 100% on site job
- Full time job
- 1 year of first contract term with expectation of continuity based on performance and budget
- Location: Salinas, PR
- Administrative shift
- Type of industry: Medical devices
About CIS International
Sourced by ZipRecruiter
Company size
11 - 50 Employees
Headquarters location
Gardena, CA, US
Year founded
1991