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Internship R&D Engineer Medical Device Jobs in Texas

KS Staffing Group

Be Seen First

Medical Device Assmbler

Richmond, TX · On-site

$22/hr

We are seeking a dedicated and detail-oriented Medical Device Assembler in the Richmond/Katy area ... Collaborate with engineering and quality assurance teams to troubleshoot assembly issues and ...

Aequor

Work with Cataract and Vitreoretinal R&D groups on development projects resulting in achieving R&D ... Experience in Medical Device industry - Manufacturing / Design / Quality Engineering fields ...

REPKON USA

Sr R&D Engineer

Garland, TX

$101K - $139K/yr

Job Title: Sr R amp;D Engineer Job Family: Engineering Company: Paligen Aerospace and Defense, LLC Location: Garland, TX Job Summary: We are seeking a detail-oriented and innovative R amp;D Engineer ...

Abbott

Title : Medical Device Tester II Location : Plano, TX Duration : 6 Months 100% Onsite Position ... The ideal candidate will collaborate cross-functionally with engineering teams to develop and ...

Medical Metrics

Full Stack Developer

Houston, TX · On-site

Medical Metrics Inc. (MMI) is a fast-growing, independent imaging core laboratory and medical ... device, biologics, and pharmaceutical companies in support of their clinical trials and product R&D.

Medical Metrics Inc

Full Stack Developer

Houston, TX · On-site

Medical Metrics Inc. (MMI) is a fast-growing, independent imaging core laboratory and medical ... device, biologics, and pharmaceutical companies in support of their clinical trials and product R&D.

A.A.D Co.

Medical Device Account Manager

Houston, TX

Residency within forty miles of the advertised location * 3 Years Prior Medical Imaging (RT(R)) or Medical Equipment/Device Sales experience * Willing to travel daily, sometimes overnight * Astable ...

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Internship R D Engineer Medical Device information

What does an Internship R&D Engineer in Medical Device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.
What cities in Texas are hiring for Internship R&D Engineer Medical Device jobs? Cities in Texas with the most Internship R&D Engineer Medical Device job openings:
Internship R D Engineer Medical Device jobs near you
Infographic showing various Internship R&D Engineer Medical Device job openings in Texas as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.
Manufacturing Engineer-Medical Device

Manufacturing Engineer-Medical Device

BioPharma Consulting JAD Group

Houston, TX

$69K - $89K/yr

Contractor

Posted 29 days ago

Job description

The Manufacturing Engineer Contractor will support the design, validation, implementation, and optimization of manufacturing processes and equipment for ophthalmic medical devices used in cataract and vitreoretinal surgeries. This role is hands-on and highly technical, with a strong focus on equipment validation, statistical process control, and continuous improvement in a regulated medical device manufacturing environment.

Key Responsibilities

  • Lead, execute, document, and manage validation activities (IQ/OQ/PQ) to support the introduction or modification of automated and semi-automated production equipment and processes.
  • Design, develop, validate, and implement manufacturing processes for ophthalmic medical devices.
  • Provide hands-on engineering support for manufacturing equipment before, during, and after release to production.
  • Apply Lean Manufacturing and Six Sigma methodologies to optimize production processes.
  • Implement Continuous Monitoring using Statistical Process Control (SPC) to maintain equipment and processes in a validated state.
  • Perform continuous statistical analysis of Critical Quality Attributes (CQAs) and process indicators to ensure compliance with product specifications (CpK / process capability).
  • Design fixtures and create technical drawings using CAD software (e.g., SolidWorks) to support daily production operations.
  • Develop and maintain standard work instructions and procedures to ensure robust and high-quality manufacturing processes.
  • Promote cross-functional collaboration through clear communication and effective coordination with all departments.

Required Skills & Competencies

  • Medical Device Validation (IQ, OQ, PQ)
  • Statistical Process Control (SPC)
  • Statistical Analysis techniques including:
    • DOE
    • ANOVA
    • Gage R&R
    • T-Test
    • Tolerance Interval Analysis
    • Control Charts
    • Process Capability (CpK)
  • Proficiency with statistical software (Minitab)
  • CAD design experience (SolidWorks or equivalent)
  • Strong technical writing skills
  • Effective public speaking and communication skills

Preferred Skills

  • Manufacturing simulation software experience (FlexSim - preferred, not required)

Requirements

Education & Experience

  • Required:
    • Bachelor's Degree in Engineering or Biomedical Engineering
    • Minimum of 1+ year of professional experience in a Medical Device Manufacturing environment
  • Preferred:
    • Master's Degree in Engineering or Biomedical Engineering

Benefits

  • 12-MONTH CONTRACT

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