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Internship Biomedical Product Development Engineer Jobs in Nevada

Work closely with Process Engineering and Manufacturing to ensure formulations can be produced ... Product Commercialization * Lead the transition of new products from development into commercial ...

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Product Development Specialist

Reno, NV ยท On-site

$50 - $70/hr

As a growing company, our engineering, manufacturing, quality, purchasing, sales, and customer ... Manage manufacturing and product development projects from initial concept through production ...

R&D Engineer

North Las Vegas, NV ยท On-site

$85 - $120/hr

Collaborate with design engineering and production/manufacturing engineering teams to transition successful R&D projects into producible designs* Stay current with emerging technologies, materials ...

Work closely with Process Engineering and Manufacturing to ensure formulations can be produced ... Product Commercialization * Lead the transition of new products from development into commercial ...

$35/hr

Shadow RA Specialists during new product development meetings to gain insight into the ... Scientific or technical disciplines preferred (e.g., Biomedical Engineering, Biological Sciences ...

New

$35/hr

Shadow RA Specialists during new product development meetings to gain insight into the ... Scientific or technical disciplines preferred (e.g., Biomedical Engineering, Biological Sciences ...

New

$35/hr

Shadow RA Specialists during new product development meetings to gain insight into the ... Scientific or technical disciplines preferred (e.g., Biomedical Engineering, Biological Sciences ...

New

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Internship Biomedical Product Development Engineer information

What does an internship biomedical product development engineer do?

An Internship Biomedical Product Development Engineer assists in designing, developing, and testing medical devices and healthcare products under the supervision of experienced engineers. Interns may participate in research, prototyping, data analysis, and documentation to support product development from concept to prototype. They often collaborate with cross-functional teams, learn industry regulations, and gain hands-on experience with tools and technologies used in biomedical engineering. This role offers valuable exposure to real-world challenges in healthcare innovation and product design.

What types of projects and responsibilities can I expect as an internship biomedical product development engineer?

As an Internship Biomedical Product Development Engineer, you will typically support product design and prototyping, conduct laboratory testing, and assist with documentation for regulatory compliance. You'll often collaborate closely with cross-functional teams, including engineers, quality assurance, and clinical specialists, to bring innovative medical devices or products from concept to early development stages. Common challenges include balancing creative problem-solving with strict regulatory requirements and managing multiple tasks to meet project deadlines. This role offers hands-on experience that can lead to full-time opportunities and valuable exposure to the entire product development lifecycle.

What are the key skills and qualifications needed to thrive as an internship biomedical product development engineer?

To thrive as an Internship Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, problem-solving, and familiarity with product development processes, typically gained through coursework or related internships. Experience with CAD software, lab equipment, and knowledge of regulatory standards such as FDA or ISO is highly valuable. Strong teamwork, communication skills, and a detail-oriented mindset help interns collaborate effectively and contribute to innovative solutions. These competencies are essential to ensure the safe, effective, and compliant development of biomedical products within multidisciplinary teams.

What is the difference between Internship Biomedical Product Development Engineer vs Biomedical Research Assistant?

AspectInternship Biomedical Product Development EngineerBiomedical Research Assistant
Required CredentialsEnrolled in or recent graduate of biomedical engineering, bioengineering, or related fieldsTypically pursuing or holding a degree in biology, biomedical sciences, or related areas
Work EnvironmentProduct development labs, engineering teams, R&D departmentsResearch labs, academic institutions, clinical research settings
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developersUniversities, research institutes, hospitals

While both roles involve biomedical sciences, the Internship Biomedical Product Development Engineer focuses on designing and developing medical devices and products, often in a corporate setting. In contrast, a Biomedical Research Assistant primarily conducts scientific research, experiments, and data analysis in academic or clinical research environments. The former emphasizes engineering and product innovation, whereas the latter centers on scientific investigation and data collection.

What are the most commonly searched types of Biomedical Product Development Engineer jobs in Nevada?

The most popular types of Biomedical Product Development Engineer jobs in Nevada are:

What are popular job titles related to Internship Biomedical Product Development Engineer jobs in Nevada?

For Internship Biomedical Product Development Engineer jobs in Nevada, the most frequently searched job titles are:

What job categories do people searching Internship Biomedical Product Development Engineer jobs in Nevada look for?

The top searched job categories for Internship Biomedical Product Development Engineer jobs in Nevada are:

Product Innovation Engineer

Origin Biologics

Las Vegas, NV โ€ข On-site

Other

Posted 7 days ago


Job description

Company Summary

Our primary mission is to provide the highest quality orthopedic implants to restore, repair, and regenerate biological and mechanical functionality lost due to degenerative diseases or trauma-related incidents. Origin Biologics, Inc. (OB) is part of the EBOS Group, a publicly listed global healthcare organization.


General Summary

The Product Development Engineer is responsible for the design, execution, and interpretation of process and product development and validation studies for HCT/Ps and medical devices. This includes supporting new product development, validation, technology transfers, process improvements, and optimization projects.


The role interacts with management, staff, suppliers, third-party laboratories, customers, and manufacturers. International travel to Australia to liaise with the Research and Engineering team will be periodically required.


Candidates must have experience in the medical device, biologics, tissue banking, or a related regulated life sciences industry.


Duties & Responsibilities

  • Support project plans and timelines for new product development.
  • Provide technical engineering support for projects and other company functions.
  • Support project planning, including budgeting, design inputs and outputs, design verification and validation, and design transfer to production.
  • Identify and define performance requirements for allograft, medical device, and instrumentation systems.
  • Support process risk activities (FMEA) for new and existing products and processes.
  • Develop verification and validation protocols and complete design verification studies.
  • Establish acceptance criteria, perform data analysis, and generate final reports.
  • Write, review, and revise QMS documentation, including policies, procedures, and forms.
  • Support concept designs and coordinate prototype manufacture.
  • Identify, coordinate, and support engineering change requests.
  • Ensure products adhere to company and industry quality standards and regulations.
  • Support process qualification and verification activities in cleanroom environments.
  • Support training activities for production personnel.
  • Perform investigations and root cause analysis for non-conformances and implement CAPAs.
  • Perform other duties and projects critical to engineering and the organization.


Experience

  • Minimum 3+ years of experience in product development, process development, validation, commercialization, or related activities within the medical device, biologics, tissue banking, pharmaceutical, or related regulated industry.
  • Experience working within regulated quality systems and product development lifecycle activities is required.


Education

๏ปฟBachelor of Science in Engineering or related scientific discipline


Certifications/Licenses

Certifications in a technical discipline relevant to the position (e.g., Certified Quality Engineer, Certified Process Validation Engineer, CTBS Certification) are not required but are considered a plus for candidates with specialized validation or quality systems experience.

Other

  • Understand the requirements of FDA 21 CFR, ISO 13485, and AATB standards.
  • Understand GLP, GMP, USP, and ISO guidelines and methodologies
  • Fundamental knowledge of aseptic techniques and principals
  • Experience with equipment/method/process validation design and acceptance criteria
  • Experience with handling biohazardous material, including human, biological and chemical samples
  • Knowledge of basic sterilization practices using steam sterilization, gamma or electron beam radiation
  • Strong technical writing skills and statistical data analysis capabilities