R&D Engineer III
Listed on 2026-02-28
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Engineering
Medical Device Industry, Biomedical Engineer, Quality Engineering, Manufacturing Engineer
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.
Job DescriptionThe Senior R&D Development Engineer will perform design and development activities on medical device/equipment products and improvements of Closure Fast products through frequent interaction with Manufacturing and Quality Engineering, Marketing, and other functions. Key responsibilities include conducting product testing and analysis on existing electrical products. You will work in a Sustaining Engineering role, improving existing endovenous products which include a generator and catheter components.
Qualifications- Bachelor's degree in Electrical Engineering, Mechanical Engineering scientific, or related technical field
- 5+ years of Engineering experience
- 3+ years of Medical device experience
- Thorough understanding of medical device industry and competitor products.
- Proficient in electrical medical device requirements, such as IEC 60601-1, IEC 60601-2
- Thorough understanding of clinical and regulatory pathways, IP and internal processes.
- In depth knowledge and wide application of technical principles, theories, and concepts in related field of expertise to develop innovative approaches to work.
- Effectively communicates and works cooperatively with others as part of a team. Shares information, status, needs, and issues with others in order to inform, gain input, and support decision-making.
- Knowledge of and ability to design reliable and innovative mechanical systems and mechanisms for consumer products.
- Knowledge of manufacturing processes.
- Proficient in Design FMECA and Design Verification and Validation activities.
- Application of statistical and analytical methods such as DOE and capability analysis.
If you are interested, please send your updated resume to (Use the "Apply for this Job" box below). call directly at .
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