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QA Supervisor - DHR Review

Penumbra, Inc. - Roseville, CA

Posted Nov 7, 2025

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 checked Jun 7, 2026
Salary
$75K-$100K Verified - from the job posting source checked Jun 20, 2026
401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$61,842 U.S. median for this role
Projected growth (BLS Employment Projections)
+1.9% - Slower

41% above the BLS role benchmark for operations aggregate.

Matched to SOC 11-1021 - Operations 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

Company

Equity
Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

QA Supervisor - DHR Review Roseville, CA As a QA Supervisor of DHR Review, you will play a pivotal role in maintaining the integrity of our Quality systems and processes. You will be responsible for supervising and overseeing DHR Review areas of the Quality System and the DHR Reviewers who work in those areas. What You'll Work On • Select, manage, train, and develop staff. Establish objectives and assignments and provide ongoing feedback through performance reviews and development plans. • Manage the scheduling of DHR Reviewers for coverage, prioritization and workload • Coordinate with internal customers to establish prioritizations and work though discrepancies • Communicate and train internal customers when processes are changed* • Complete DHR Review when needed • Analyze and generate trending data to support system effectiveness • Evaluate procedures and work instructions for processing improvements and implement changes as necessary • Support Quality System processes during internal and external regulatory audits • Proactively seek system improvements while maintaining compliance to applicable requirements. • Communicate Quality System issues to upper management, presenting solutions as appropriate What You Contribute • A Bachelor's degree with 2+ years of experience, or equivalent combination of demonstrated education and experience • Proficiency with Microsoft Office (e.g., Word, Excel, Access, PowerPoint, etc.) • Demonstrated working knowledge of Medical Device regulations • Prior supervisory experience preferred • Solid problem solving, decision-making, and supervisory skills required • High degree of accuracy and attention to detail • Excellent organizational skills with ability to prioritize assignments while handling

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