R&D Engineer II

Ledgent Technology; Irvine (CA); On-site; USD 55,000 - 60,000; Part time

Job summary

Roth Staffing is seeking an R&D Engineer II for a medical device manufacturing company. This 12-month contract role offers an hourly pay rate of $40.00 to $43.72, starting immediately.

The engineer will support THV delivery systems, lead design control activities, and coordinate cross-functional teams to drive product development and improvements. Responsibilities include applying design controls, performing risk assessments, and contributing to verification and validation efforts.

Qualifications

• Bachelor's or Master's degree in engineering or sciences with required years of experience.
• Experience in life sciences or medical device industry is preferred.
• Experience with design controls, V&V, and risk management.

Responsibilities

• Provide engineering input to THV product projects applying design controls and risk management.
• Lead investigations into field performance issues and support labeling and training updates.
• Develop test methods and procedures to evaluate device prototype performance.
• Maintain documentation and generate protocols, reports, and technical summaries.

Skills

Design controls

Quality engineering

Statistical analysis

Independence

Cross-functional collaboration

Education

Bachelor's Degree in engineering or scientific field

Master's Degree in engineering or scientific field

Tools

Statistical software

Job description

Salary: USD40 - USD43.72 per hour

Roth Staffing is looking for a R&D Engineer II for Medical Device Manufacturing company. Duration: 12 months contract to start with potential to extend. Hourly Pay Rate: $40.00 -or- $43.72

The E2 R&D Engineer will play a key role in support of transcatheter aortic valve therapies. This role is responsible for leading and supporting key projects associated with our commercialized THV products. This includes support of product configuration changes, providing design control expertise for supply-chain driven manufacturing improvements, leading investigations into field performance issues and support of product labeling and training updates associated with our global therapy expansion.

Essential Job functions include:

• Provide Engineering input to THV commercialized product projects including application of design control and risk management Develop solutions to a variety or problems of moderate scope and complexity.


• Be a subject matter expert on field performance of THV devices and the design features associated with key performance metrics


• Apply mechanical and biomedical engineering principles to the design and development of components for the delivery system and accessories.


• Adaptable to broad scope of projects including material changes, manufacturing improvements, packaging and labeling changes, use instruction and usability changes. Develop test methods and procedures to evaluate device prototype performance.


• Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinate technician work.


• Build partnerships with key cross functional stakeholders


• Maintain accurate documentation of concepts, designs, drawings, and procedures. Generate written protocols, reports, and technical justifications/summaries.


• Other incidental duties assigned by Leadership

Required Qualifications:

• Bachelor's Degree required in an engineering or scientific field, plus (4) years of experience in quality engineering; OR Master’s Degree in engineering or scientific field, with (3) years of experience in quality engineering


• Lifesciences industry experience (i.e. medical device, pharma, or biotech)


• Experience with design controls, design verification & validation, or design test method development


• Demonstrated experience reviewing and updating risk management related documents


• Experience utilizing statistical techniques to support design decisions and product acceptance testing


• Experience in new product development with successful design experience from concept to commercialization is strongly preferred.


• Effective communication, listening, and diagnostic skills, verbal and written, are necessary. The demonstration of effective collaboration and influencing skills will be key so that the candidate can achieve results within the cross-functional team and with stakeholders around the company.


• Ability to work well independently and as a member of a team is essential.

Preferred Qualifications:

• Master's Degree in an engineering, scientific or a related discipline


• Medical device industry experience highly preferred.


• Experience in catheter-based therapies preferred.


• Design control and design change experience for product improvements


• Experience with sustaining activities for commercialized products


• Strong experience in quality engineering, R&D or manufacturing engineering


• Design for Six Sigma or Lean Six Sigma Certification (Green belt or black belt)


• Working knowledge and understanding of statistical techniques


• Previous experience working with test lab equipment required (if applicable)


• Strong problem-solving, organizational, analytical and critical thinking skills


• Good leadership skills and ability to influence change


• Knowledge of Design Control


• Knowledge of applicable FDA regulations for medical device industry desirable


• Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on contracts or projects