Mendaera, Inc.

Mendaera, Inc.

Incoming & Manufacturing Quality Technician

San Mateo, CA · Mid

Sponsorship not specified$95k-$115kDetected 13 days ago
ExcelSupply ChainERPRoboticsGMPFDA RegulatoryMedical DevicesMicrosoft OfficeRegulatory Affairs

Stay score

odds of building a lasting career here

47Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
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.

Personalize to your clock →

H-1B wage level

the lottery is wage-weighted — each level is one more entry

Level I · 1×
Level I$96,0961 entry
Level II$117,6242 entries
Level III$139,1313 entries
Level IV$160,6594 entries

The bottom of this range ($95,000) is below the Level I prevailing wage of $96,096. An H-1B cannot be filed below the prevailing wage, so an offer at the floor of this band could not be sponsored as posted.

DOL prevailing wage, 2026-27 wage year · Industrial Engineers (17-2112) · San Francisco-Oakland-Fremont, 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

Files H-1B transfers

2 transfer filings in the last year, covering 2 workers. Median labor-condition decision: 24 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.

Community outcomes

No reports yet — be the first to help the next applicant.

About the role

  • Physical Demands - Able to work in a fast-paced production environment. - Ability to lift and handle objects up to 20 pounds.

Responsibilities

  • Perform incoming inspection of purchased materials, components, and assemblies using approved inspection procedures and sampling plans.
  • Support manufacturing through in-process and in-line inspections to verify compliance with approved procedures and quality standards.
  • Identify, document, and segregate nonconforming materials; initiate and support Nonconformance Reports (NCMRs) and Material Review Board (MRB) activities.
  • Support product release activities, rework verification, engineering builds, and continuous improvement initiatives.
  • Collaborate with Manufacturing, Engineering, Supply Chain, Supplier Quality, and Regulatory Affairs to resolve quality issues and support production.
  • We are looking for candidates who thrive in fast-paced environments, embrace ambiguity, can support the development of frameworks and work products, are willing to engage in both detailed and broader-level analysis, possess critical and systems-thinking abilities, and are detail-oriented.
  • Identify, document, and segregate nonconforming materials
  • initiate and support Nonconformance Reports (NCMRs) and Material Review Board (MRB) activities.
  • Process-oriented with the ability to plan and perform work.

Requirements

  • Ability to lift and handle objects up to 20 pounds.
  • Required Skills and Experience
  • Experience with eQMS and ERP systems.

Nice to have

  • Review supplier documentation, engineering drawings, specifications, and acceptance criteria.
  • Conduct visual, dimensional, and functional inspections using calibrated inspection equipment.
  • Review Device History Records (DHRs), travelers, Manufacturing Process Instructions (MPIs), and related production documentation for accuracy and completeness.
  • Coordinate equipment calibration, preventive maintenance, and equipment status while maintaining calibration records.
  • Ensure compliance with FDA QMSR (21 CFR Part 820), ISO 13485, Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP).
  • Fulfill any other duties as assigned.
  • Minimum 2+ years of quality inspection experience in a regulated manufacturing environment.
  • Working knowledge of common inspection tools.

Compensation

  • $95,000 to $115,000 (this is an hourly position)

Benefits

  • Mendaera is developing technology that will enable all healthcare providers to do more for their patients.
  • Experience in medical device manufacturing preferred.

Company info

  • Our aim is to eliminate barriers in the patient journey, accelerate recovery, delight customers, and reduce cost of care.

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