Stryker
Staff Quality Compliance Engineer
Irvine, California · Staff+ · Contract
Stay score
odds of building a lasting career here
Sponsors, but it's cap-subject — you still face the weighted lottery (~45% per draw at Level III). Good if you win; have a cap-exempt backup on your list.
Lottery odds assume a STEM candidate.
Personalize to your clock →H-1B wage level
the lottery is wage-weighted — each level is one more entry
$14,591 more — $117,291 — moves this role to Level IV and 4 lottery entries. That figure is inside the range the employer already advertised.
Based on the DOL prevailing wage for this occupation and worksite, a base salary of $117,291 would place this position at wage Level IV. That figure is within the posted range, and I'd like to target it. This role classifies under "Compliance Officers" for prevailing-wage purposes.
DOL prevailing wage, 2026-27 wage year · Compliance Officers (13-1041) · Los Angeles-Long Beach-Anaheim, CA. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.
Employer immigration record
from this employer's Department of Labor filings
Green-card follow-through: 50%
Files H-1B transfers
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 Flexibility: Onsite Staff Quality Compliance Engineer Irvine, CA Join Stryker in a key role supporting global regulatory compliance across the product lifecycle.
- Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.
- Stryker is an EO employer - M/F/Veteran/Disability.
Responsibilities
- Lead the Standards & Regulations Management Compliance program as the Division Process Owner, aligning processes and compliance activities across divisions.
- Develop and implement compliance action plans to maintain product and quality system conformity.
- Support internal and external audits as a subject matter expert and review technical documentation, test protocols, and reports for regulatory conformity.
- The role partners closely with cross-functional teams to assess regulatory changes, evaluate impact, and implement compliance actions across products and processes.
Requirements
- Bachelor's degree in Engineering, or related discipline.
- Minimum 4 years of experience in regulatory compliance, quality, engineering, or a related function.
- Experience performing regulatory impact assessments and standards gap analyses.
- Experience with design controls, risk management, and quality management systems.
- Partner with cross-functional teams to execute compliance activities and ensure required documentation is completed according to company procedures.
Nice to have
- Experience supporting internal and external regulatory or quality audits.
- Travel Percentage: None
- Stryker Corporation is an equal opportunity employer.
Compensation
- $102,700 - $171,100 USD Annual
Benefits
- Monitor and identify new or revised global regulatory requirements, standards, and guidance applicable to medical devices and quality systems.
- Experience working within the medical device, healthcare, or regulated industry.
- This position provides technical leadership for standards and regulations management, ensuring medical device products and quality systems remain aligned with evolving global regulatory requirements.
- Knowledge of global medical device regulations and international standards.
This listing is sourced directly from Stryker's careers page and normalized into a canonical job model.