Quality Operations Engineer

Posted 8 Days Ago
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Lodi, CA, USA
In-Office
71K-85K Annually
Junior
Biotech
The Role
The Quality Operations Engineer supports Manufacturing Quality activities by maintaining QMS compliance, supporting investigations, and driving process improvements.
Summary Generated by Built In

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cepheid, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. 

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world’s most complex health challenges. Together, we bring MORE change to the world.

Learn about the Danaher Business System which makes everything possible.

The Quality Operations Engineer supports day-to-day Manufacturing Quality activities by completing structured assignments using established procedures and under the guidance of senior Quality Engineering staff to help maintain compliance with the Quality Management System (QMS) and applicable regulations. This role contributes to product quality and sustaining operations by supporting investigations, documentation updates, and process improvement activities.

This position reports to the Manager, Manufacturing Quality and is part of the Cepheid Quality Operations Team located in Lodi, California. This is an ON-SITE role supporting twenty-fourx7 manufacturing operations.

Schedule: 5 days (Monday - Friday) – Day Shift

In this role, you will have the opportunity to:

  • Quality point of contact assisting with day-to-day inquiries and escalations; gather information, document issues, and escalate to senior Quality/Manufacturing leadership as needed.
  • Participate in quality system and process improvement activities by collecting data, performing trending, and supporting GEMBA and problem-solving activities using established tools and templates.
  • Work with engineering and manufacturing teams to support process improvements and variability reduction by executing assigned tasks (e.g., data collection, document updates, and follow-up actions) under guidance.
  • Support process validations, process control plans, and statistical process control (SPC) activities by following documented protocols/work instructions and accurately recording results.
  • Support project teams by updating and maintaining quality documentation (e.g., inspection and manufacturing documents, test methods, and Device History Records (DHRs)) using established templates and review processes.
  • Support compliance activities related to design control and change control by preparing documentation, routing records for review/approval, and following established procedures.

The essential requirements of the job include:

  • Bachelor’s degree in an engineering or related field (e.g., Industrial, Biomedical, Molecular Biology, Mechanical), with 0–2 years of related experience (internship/co-op experience may be considered)
  • Foundational understanding of quality concepts and tools (or demonstrated ability to learn them quickly) and the ability to follow documented procedures in a regulated environment

It would be a plus if you also possess previous experience in:

  • Exposure to medical device or diagnostics regulations/standards (e.g., 21 CFR Part 820 and ISO 13485) and interest in learning how they are applied in manufacturing quality.
  • Experience working at a manufacturing facility (preferably high volume)
  • A quality engineering certification from the American Society for Quality (ASQ), or other qualifying organizations. Examples may include but are not limited to the CQE, CRE, CQA, etc.

Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

At Cepheid we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cepheid can provide.

The annual salary range for this role is $70,500 – 85,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

#LI-LCS

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [email protected].

Skills Required

  • Bachelor's degree in engineering or related field
  • 0-2 years of related experience (internship/co-op experience may be considered)
  • Foundational understanding of quality concepts and tools

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

Cepheid Insights

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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