R&D Engineer II

Cordis

$78K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical, Biomedical, or Chemical Engineering.
  • 3+ years in medical device product development or relevant education and experience.
  • Strong knowledge of design controls and risk management.
  • Proficiency with SolidWorks or equivalent CAD software.
  • Experience with combination product development (preferred).
  • Familiarity with balloon catheter manufacturing or coating processes (preferred).

Responsibilities

  • Execute product and process development activities including design, testing, and analysis.
  • Support development and execution of design verification and validation protocols.
  • Prepare and maintain design documentation, including drawings, specifications, and reports.
  • Perform failure analysis and recommend design or process improvements.
  • Collaborate with Manufacturing, Quality, and Analytical teams to ensure robust design transfer.
  • Support regulatory submissions by providing engineering documentation and test data.
  • Participate in risk assessments and implement design mitigation strategies.
  • Contribute to continuous improvement of design and development processes.

Benefits

  • Comprehensive health and wellness programs.
  • Professional development opportunities.
  • Collaborative and innovative team environment.
  • Access to state-of-the-art laboratory facilities.
  • Potential for impact in transforming patient care.
Full Job Description
Responsibilities

We are seeking a talented and motivated R&D Engineer II to join our dynamic team of innovators in Irvine, California. As an R&D Engineer, you will play a pivotal role in the development and enhancement of our combination medical devices. Working closely with a multidisciplinary team, you will contribute to the design, prototyping, testing, and validation of innovative medical devices that have the potential to transform patient care.

Key Accountabilities
  • Execute product and process development activities including design, testing, and analysis.
  • Support development and execution of design verification and validation protocols.
  • Prepare and maintain design documentation, including drawings, specifications, and reports.
  • Perform failure analysis and recommend design or process improvements.
  • Collaborate with Manufacturing, Quality, and Analytical teams to ensure robust design transfer.
  • Support regulatory submissions by providing engineering documentation and test data.
  • Participate in risk assessments and implement design mitigation strategies.
  • Maintain compliance with ISO 13485, FDA 21 CFR Part 820, and company procedures.
  • Contribute to continuous improvement of design and development processes.


Qualifications

Required Qualifications
  • Bachelor's degree in Mechanical, Biomedical, or Chemical Engineering.
  • 3+ years of experience in medical device product development or combination of education and experience.
  • Strong knowledge of design controls and risk management principles.
  • Proficiency with SolidWorks or equivalent CAD software.


Preferred Qualifications
  • Experience with combination product development.
  • Familiarity with balloon catheter manufacturing or coating processes.


Key Competencies
  • Technical proficiency and attention to detail.
  • Strong analytical and communication skills.
  • Ability to manage multiple priorities in a collaborative environment.
  • Problem-solving and continuous improvement mindset.


Working Conditions
  • Laboratory and office environment.
  • May require standing or bending for extended periods.
  • Light lifting (up to 25 lbs.)


Preferred Qualifications

Pay / Compensation
The expected pre-tax pay rate for this position is $78,650 - $105,600 per year. Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.

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