R&D Engineer II
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Job Location:
Irvine, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
5 hours ago
Vacancies:
1 Vacancy
Job Summary
Key Responsibilities
- Contribute to the development and launch of new drug/medical device combination products.
- Independently design execute and interpret novel engineering research and development.
- Generate and lead new engineering proposals. Investigate identify develop and optimize new test methods and techniques and set and meet experimental timelines. Innovate and implement new experimental protocols.
- Act as a critical contributor to feasibility development and verification testing stages of product development through creation and release of new test methods as well as design verification plans protocols records and reports.
- Effectively organize and present scientific plans and data. Contribute to writing and conceptual framework of publications presentations and patents.
- Act as a resource or mentor for others.
Qualifications :
Education & Experience
Must possess a Masters Degree in Industrial and Systems Engineering Mechanical Engineering Biomedical Engineering or a related field and 1 year of experience in the job offered or in a regulated device engineering or validation-related occupation. Requires 1 year of experience involving the following: 1. Regulated device testing processes including detailed verification and validation methodologies; 2. Experience with design control risk management and regulatory standards including ISO FDA and ASTM standards; 3. Developing managing and maintaining complex technical drawings and designs utilizing SolidWorks or a similar 3D CAD design software; 4. Demonstrated problem-solving skills for effectively identifying analyzing and resolving technical issues to ensure project success and product quality; 5. Quality assurance processes for ensuring comprehensive compliance and maintenance of high standards throughout development and testing; 6. Advanced Data analytics for conducting analyses and deriving actionable insights for informed decision making; and 7. Project management.
Additional Information :
Salary: $102877 - $157500 per year
Apply online at or send resume to . Refer to Req ID: REF49220X
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term and long-term incentive programs.
AbbVie is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- Laboratory Experience
- Vendor Management
- Design Controls
- C/C++
- FDA Regulations
- Intellectual Property Law
- ISO 13485
- Research Experience
- SolidWorks
- Research & Development
- Internet Of Things
- Product Development
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
