Penumbra

Quality Engineer II

Alameda, CA · Mid

Sponsorship not specified$95k-$127kDetected 91 days ago

ExcelIntellectual PropertyMedical DevicesCommunicationMicrosoft Office

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odds of building a lasting career here

50Sponsors, lottery-bound

Cap-exempt (no lottery)0

Sponsors this role90

Entry-level history0

PERM / green-card track0

Lottery odds (Level II)66

Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~30% per draw at Level II). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 12 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 78%

Of 9 labor certifications old enough to have been used, 2 expired without the employer filing the next step. Median time from filing to decision: 491 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Files H-1B transfers

8 transfer filings in the last year, covering 8 workers. Median labor-condition decision: 8 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

Work with problems of moderate scope where the analysis of situation or data requires a review of identifiable factors.
Exercise judgment to determine appropriate action.
Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies.

Responsibilities

Collaborate in the development and qualification activities for new and existing products*
Collaborate in the development of testing and inspection methodology and documentation for new and existing products*
Collaborate on Quality Objective teams*
Design and install QC process sampling systems, procedures, and statistical techniques*
Design or specify inspection and testing mechanisms and equipment*
Perform failure analyses and defect investigations *
Collaborate in the development of standard operating procedures*
Facilitate and perform internal audits*

Requirements

Associate's or Bachelor's degree in Engineering, a Life Science, or a related field, with 2+ years of quality engineering or relevant experience, preferably in a medical devices or regulated industry environment, or equivalent combination of education and experience.

Nice to have

Familiarity with QSR, ISO and other applicable regulations and laws required
Experience with Electronic devices and or PCBAs
Excellent verbal, written, and interpersonal communication skills
Proficiency with MS Word, Excel, and PowerPoint Working Conditions
General office, laboratory, and cleanroom environments
Potential exposure to blood-borne pathogens
Requires some lifting and moving of up to 25 pounds
Must be able to move between buildings and floors.

Compensation

$95,000 to $127,000 We offer a competitive compensation package plus a benefits and equity program, when applicable.
Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

Company info

Interface with other engineering departments within the company, customers, and suppliers on quality related issues*

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This listing is sourced directly from Penumbra's careers page and normalized into a canonical job model.