Quality Engineer I

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified

Salary

$72K-$94K not verified - source not recorded; timestamp not recorded

401(k) match

Not verified

Was this benefit information wrong? Tell us.

Market context

U.S. role benchmark (BLS OEWS)

$111,944 U.S. median for this role

Projected growth (BLS Employment Projections)

+13.7% - Much faster than average

26% below the BLS role benchmark for data and ml aggregate.

Matched to SOC 15-1252 - Data and ML aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type

Not verified

Weekend work

Not verified

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Quality Engineer I Roseville, CA General Summary As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements. What You'll Work On •Provide valuable input in the design control process and help in developing and launching new products •Independently provide knowledge of Penumbra Quality Management System as it pertains to sustaining manufacturing operations as well as dealing with supplier quality and developing new products •Identify and drive areas of opportunity for process improvement, yield improvement, and cycle time reduction •Determine root-cause of in-process quality assurance issues •Experience on production lines manufacturing high performing products •Adhere to the Company's Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. •Ensure other members of the department follow the QMS, regulations, standards and procedures. •Perform other activities requiring knowledge of principles and techniques commonly employed in the specific area of projects. What You'll Bring •1+ years of experience in a manufacturing or laboratory environment strongly preferred •Proven ability to thrive in a fast-paced work environment where navigating grey areas is a welcomed

Read the full description at jobs.lever.co. FewerJobs shows a preview and links to the original posting.