R&D Engineer II

BioSpace; Irvine (CA); On-site; USD 102,877 - 157,500; Full time

Benefits offered by this job

Paid time off

Medical, dental, and vision insurance

401(k) plan

Job summary

A leading healthcare company in California is seeking an Engineering professional to contribute to the development of innovative drug and medical device combinations. The role requires a Master's Degree in relevant engineering fields and experience with regulatory device testing processes. Candidates should possess strong problem-solving skills and be proficient with design control and project management. This position offers a competitive salary and comprehensive benefits package, including health insurance and 401(k).

Qualifications

• Must have 1 year of experience in device testing with verification and validation methodologies.
• Experience with ISO, FDA, and ASTM regulatory standards.
• Demonstrated ability to resolve technical issues for project success.

Responsibilities

• Contribute to development and launch of new drug/medical device combinations.
• Design, execute, and interpret novel engineering research.
• Organize and present scientific plans and data effectively.

Skills

Problem-solving skills

Project management

Data analytics

Quality assurance processes

Experience with design control

Education

Masters Degree in Industrial and Systems Engineering, Mechanical Engineering, or Biomedical Engineering

Tools

SolidWorks or similar 3D CAD software

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Job Description

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.


7. Project management.

Additional Information

Salary: $102,877 - $157,500 per year

Apply online at https://careers.abbvie.com/en or send resume to [e-mail]. 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 AbbVie's 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html