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Entry Level Quality Engineer information

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$44.4K

$82.9K

$117.4K

How much do entry level quality engineer jobs pay per year?

As of Jul 19, 2026, the average yearly pay for entry level quality engineer in California is $82,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,100.00 and $91,800.00 per year, depending on experience, location, and employer.

What types of projects or tasks can I expect to work on as an Entry Level Quality Engineer?

As an Entry Level Quality Engineer, you will typically be involved in tasks such as performing inspections, collecting and analyzing data on product quality, assisting in root cause analysis for defects, and supporting process improvement initiatives. You may also help implement quality standards, work closely with production teams to resolve issues, and participate in audits or compliance activities. The projects you work on will often require collaboration with manufacturing, design, and supply chain teams, giving you exposure to various aspects of the production process. This variety helps build foundational skills and experience, setting the stage for future career advancement within the quality or engineering departments.

What are the key skills and qualifications needed to thrive in the Entry Level Quality Engineer position, and why are they important?

To thrive as an Entry Level Quality Engineer, you need a solid understanding of engineering principles, attention to detail, and a bachelor's degree in a relevant field such as mechanical or industrial engineering. Familiarity with quality management systems (like ISO 9001), data analysis tools, and software such as Minitab or Microsoft Excel is commonly required. Strong communication, problem-solving skills, and the ability to work collaboratively are key soft skills in this position. These skills ensure you can effectively identify and resolve quality issues, drive process improvements, and contribute to overall product reliability and customer satisfaction.

What is an Entry Level Quality Engineer job?

An Entry Level Quality Engineer is responsible for ensuring products or processes meet quality standards and regulatory requirements. They assist in inspecting products, analyzing defects, and implementing quality control procedures. Their role often includes working with production teams to identify and fix issues, documenting test results, and contributing to process improvements. Strong analytical skills, attention to detail, and knowledge of quality standards like ISO or Six Sigma are beneficial. This position serves as a foundation for advanced roles in quality engineering and manufacturing.

What are the most commonly searched types of Quality Engineer jobs in California? The most popular types of Quality Engineer jobs in California are:
What are popular job titles related to Entry Level Quality Engineer jobs in California? For Entry Level Quality Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Entry Level Quality Engineer jobs in California look for? The top searched job categories for Entry Level Quality Engineer jobs in California are:
What cities in California are hiring for Entry Level Quality Engineer jobs? Cities in California with the most Entry Level Quality Engineer job openings:
Entry Level Quality Engineer jobs near you
Infographic showing various Entry Level Quality Engineer job openings in California as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $82,939 per year, or $39.9 per hour.
Supplier Quality Engineer

Supplier Quality Engineer

Katalyst Healthcares & Life Sciences

Sunnyvale, CA

Contractor

Re-posted 28 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Responsibilities:

  • Select and evaluate suppliers by leading efforts to find new suppliers in an existing or new commodity.
  • Conduct on-site supplier assessments as well as QMS audits and address the non-conformities.
  • Work with suppliers and ISI engineering for the new product introduction to
  • Complete part production qualification process ( PPQP), which includes but not limited to delivering on the following deliverables: spFMEA, Special Process Validations, Process capability, MSA, capacity analysis, and FAIR.
  • Develop supplier ramp readiness based on forecast, supplier capacity, quality performance, and process capability.
  • Perform DFM by engaging suppliers early in development cycle to feedback manufacturability improvements in the designs prior to production.
  • Lead and resolve the supply continuity/ quality issues at suppliers through in depth root cause and corrective actions utilizing SCARs, SCRs (Supplier Change requests) processes.
  • Monitor supplier performance and initiate improvement activities.
  • Drive suppliers to continually improve their business and manufacturing process performance to meet Intuitive Surgical's requirements for supplier excellence including ship to stock programs using a collection of best practices in project management, Six Sigma, Lean, SPC and negotiation by leading these efforts without managerial guidance at several suppliers simultaneously.
  • Develop and use metrics for supplier part cost, delivery, quality, capacity and capability by creating metrics to measure real improvement and judge required intervention or change at the supplier or in a commodity.
  • Driving change to ISI specifications as necessary by understanding and changing specifications and drawings including driving the ECO process to implementation.
  • Prepare and deliver supplier communications as required by independently working with suppliers on scorecard creation of QBRs, Supplier Summits, etc.
  • Identify and investigate opportunities for cost reduction and/or quality improvement by judging opportunities and creating strategies to seize those opportunities, completes research and provides data-driven plans to management.

Requirements:

  • BS degree in Engineering or equivalent, master's degree preferred.
  • Excellent knowledge of 21 CFR part 820 and ISO 13485 (experience in auditing suppliers to these standards): Certified Lead auditor preferred but not required.
  • Practical knowledge of PFMEA's and process validations.
  • Ability to read and interpret detailed mechanical drawings and communicate technical information.
  • Excellent problem solving and project management skills.
  • Excellent written and verbal communication skills including presentations to executive level management.
  • A proven history of implementing Lean/6 Sigma/SPC Programs at suppliers.
  • Practical knowledge of part production qualification process.
  • Significant computer experience using Windows, Word, Excel, Access and ERP Information Systems, preferably SAP.
  • CAD experience with 3D modelling tools is a plus.
  • Experience in a high-volume medical device company is a plus.
  • Ability to travel to suppliers on an as needed basis - domestic and international.
Additional Information

All your information will be kept confidential according to EEO guidelines.

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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