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Sr. Quality Assurance Engineer

ZEISS · Dublin, CA

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Level
Senior
Team
Quality
Base pay
$116k–$145k
Degree
Required
Experience asked
79+ years
Industry
Industrial
Posted
Yesterday

The role in 30 seconds

A senior quality role at ZEISS (industrial) in Dublin, CA. It is not to be construed as an exhaustive statement of requirements, duties, or responsibilities.

They ask for
79+ years · degree required
Tools it names
Root cause, CAPA, ISO 13485, FDA / GMP
Base pay
$116k–$145k

Read from the posting. The full description is below.

From the plant jobs report · week of October 26, 2026

Quality Engineer roles in California: typical posted base $101k–$148k. This one lists $116k–$145k.

Median of the low and high ends of 97 live postings that list pay, out of 197 quality engineer openings in California, read from manufacturers' own careers sites.

California plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 196 other live quality postings in California.

Base pay
About 5% above similar roles

Typical $100k–$148k, from 94 postings that list pay.

Experience asked
More than usual (79+ vs 5+)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • ✓ Root cause 78%
  • FMEA 54%
  • Supplier quality 48%
  • Validation (IQ/OQ/PQ) 46%
  • AS9100 42%
  • ISO 9001 38%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for ISO 13485, FDA / GMP, which few similar roles mention. If you have it, lead with it.

It asks for 79+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at ZEISS

    We found 5 people at this company and state: 4 in this kind of role, 1 leaders. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to M. → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: ZEISS in Dublin

2 other open roles at this site · 5 people we found in quality roles at ZEISS.

Full description from ZEISSAs posted on their careers site.Show

requirements

into quality objectives, and drive risk-based improvements. The position also manages escalated product complaints, coordinates investigations and root-cause analyses, evaluates potential regulatory reporting obligations, and ensures complete and timely complaint closure.

Location: Dublin, CA

Sound Interesting?

requirements

for this job. It is not to be construed as an exhaustive statement of requirements, duties, or responsibilities. The Company reserves the right to interpret, amend, or otherwise modify, in whole or in part, any job description at any time, at its sole discretion.

Show full description ↓

About Us

How many companies can say they’ve been in business for over 179 years?!

Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team!

What’s the role?

The Senior Quality Assurance Engineer provides quality leadership for assigned product families throughout the product lifecycle. This role partners with Product Management, R&D, Operations, Service, and Purchasing to monitor product and process performance, translate customer and regulatory

Here’s what you’ll do

  • •Provide quality engineering support for manufacturing, purchasing, R&D, and product-sustaining activities.
  • •Serve as the Quality Assurance representative and subject-matter expert for assigned product families.
  • •Develop and monitor product and process quality metrics, identify adverse trends, and lead appropriate improvement activities.
  • •Apply statistical methods to product acceptance, process capability, sampling, data analysis, and performance evaluation.
  • •Support product and process changes by assessing quality, regulatory, and risk-management impacts.
  • •Lead or support complex quality investigations, root-cause analyses, corrective actions, and effectiveness evaluations.
  • •Manage escalated product complaints and ensure that complaint records are complete, accurate, traceable, and properly maintained.
  • •Assess complaint classification, potential regulatory reporting obligations, and the need for further investigation, risk evaluation, or quality action.
  • •Coordinate complaint investigations, returned-product evaluations, regulatory reporting inputs, stakeholder communication, and timely closure.
  • •Support the maintenance and continuous improvement of the Quality Management System.
  • •Lead quality projects and provide technical guidance and training to other personnel.
  • •Support regulatory inspections and internal or external audits, as required.

Do you qualify?

  • •Bachelor’s degree in engineering, science, or a related technical discipline.
  • •Minimum five years of relevant experience in quality assurance, product development, manufacturing quality, or failure analysis within a regulated industry.
  • •Working knowledge of ISO 13485, FDA Quality Management System Regulation under 21 CFR Part 820, and applicable U.S. and EU medical device requirements.
  • •Experience with complaint investigations, root-cause analysis, CAPA, risk management, and quality-system processes.
  • •Proficiency in statistical methods, including sampling, process capability, confidence intervals, data-distribution assessment, and interpretation of quality data.
  • •Demonstrated ability to lead multiple complex projects and work effectively across functions.
  • •Strong written and verbal communication skills.
  • •Ability to adapt and make sound decisions in a changing environment.
  • •Experience with medical electronic, ophthalmic, optical, or similar regulated products is preferred.

The annual pay range for this position is $115,900 - $144,900.

The pay offered for this role may be influenced by factors such as job location, scope of role, qualifications, education, experience, & complexity/specialization/scarcity of talent.

This position is eligible for a Performance Bonus.

ZEISS also offers robust benefits, including medical plans, retirement savings plan and paid time off.

We have amazing benefits to support you as an employee at ZEISS!

  • •Medical
  • •Vision
  • •Dental
  • •401k Matching
  • •Employee Assistance Programs
  • •Vacation and sick pay
  • •The list goes on!

The above is intended to describe the general content of and

Your ZEISS Recruiting Team

Jo Anne Mittelman

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