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Internship Septic Design Engineer Jobs in Riverside, CA

Marvell

Principal Design Verification Engineer

Irvine, CA · On-site

$146K - $178K/yr

... design of state-of-the-art multi-core SoCs. Transforming the requirements from the engineering ... every stage - from internship to retirement and through life's most important moments. Our ...

Marvell

Sr. Staff Design Verification Engineer

Irvine, CA · On-site

$146K - $178K/yr

... design/simulation environment automation. * Hardware/Firmware interaction and Firmware programming ... every stage - from internship to retirement and through life's most important moments. Our ...

Danaher

Software Engineer Internships

Pomona, CA · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... Participating on an Agile Scrum team, collaborating across design, development, and testing

Council on American-Islamic Relations

Internship

Anaheim, CA · On-site

$15.75 - $21/hr

Interns assist with implementing CAIR's youth programming with a focus on the issues of identity ... Graphic and Web Design: Responsibilities include the development and maintenance of the CAIR-CA ...

Danaher

Software Automation Internships

Pomona, CA · On-site

This potential opportunity could offer hands-on experience as part of an Agile engineering team, contributing to process automation, testing strategies, and design optimization. Interns in similar ...

Infinite Peripherals

Sustaining Engineer I

Irvine, CA · On-site

$80K - $88K/yr

Support the Lead Engineer with design, prototyping, and documentation tasks in SolidWorks and ... internships. * Manufacturing Knowledge: Understanding of manufacturing processes such as plastic ...

Infinite Peripherals

Sustaining Engineer I

Irvine, CA · On-site

$80K - $88K/yr

Support the Lead Engineer with design, prototyping, and documentation tasks in SolidWorks and ... internships. * Manufacturing Knowledge: Understanding of manufacturing processes such as plastic ...

RimePro Inc

Jr. Plumbing Engineer

Corona, CA

$60K - $80K/yr

Participate in project meetings and site walks as needed Qualifications * 1-3 years of plumbing design experience (internships included) * Associate's or Bachelor's degree in Mechanical Engineering ...

RimePro Inc

Jr. Plumbing Engineer

Norco, CA · On-site

$60K - $80K/yr

Participate in project meetings and site walks as needed Qualifications * 1-3 years of plumbing design experience (internships included) * Associate's or Bachelor's degree in Mechanical Engineering ...

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All JobsSeptic Design Engineer JobsInternship Septic Design Engineer JobsInternship Septic Design Engineer Jobs in Riverside, CA

Internship Septic Design Engineer information

See Riverside, CA salary details

$9

$20

$38

How much do internship septic design engineer jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for internship septic design engineer in Riverside, CA is $20.22, according to ZipRecruiter salary data. Most workers in this role earn between $15.05 and $22.55 per hour, depending on experience, location, and employer.

What is the difference between Internship Septic Design Engineer vs Septic Design Engineer?

AspectInternship Septic Design EngineerSeptic Design Engineer
CredentialsEnrolled in or recent graduate of civil/environmental engineeringBachelor's or higher in civil/environmental engineering, with experience
Work EnvironmentInternship setting, assisting senior engineers, learning-focusedFull-time professional role, responsible for designing septic systems
ResponsibilitiesSupporting design tasks, research, learning industry standardsCreating septic system designs, calculations, client communication

The main difference is that an Internship Septic Design Engineer is a learning position for students or recent graduates gaining industry experience, while a Septic Design Engineer is a full-time professional responsible for designing septic systems independently. Internships focus on training and skill development, whereas full engineers handle project execution and client interactions.

What cities near Riverside, CA are hiring for Internship Septic Design Engineer jobs? Cities near Riverside, CA with the most Internship Septic Design Engineer job openings:
Internship Septic Design Engineer jobs near you
Engineer II, R&D Sustainment

Engineer II, R&D Sustainment

Edwards Lifesciences Corporation

Irvine, CA • On-site

Full-time

Posted 25 days ago

Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

65th of 528 rated manufacturers

Job description

Innovation starts from the heart. At Edwards, we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease. As part of our R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients' lives around the world.
Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
How you will make an impact:
The Engineer II, R&D Sustaining will support lifecycle management of on-market Class III medical devices by investigating field and manufacturing issues, developing automated tools to monitor device performance, implementing design and process improvements, supporting engineering change assessments, and ensuring continued product safety, performance, reliability, manufacturability, and regulatory compliance.
The role is ideal for an engineer who enjoys working across the boundary between device hardware and data systems, with data-driven investigations, cross-functional collaboration, and ownership of product performance after commercial release. The successful candidate will use engineering judgement, data analysis, algorithm development, design control principles, risk management practices, and verification and validation methods to support product improvements, automated monitoring, and high standards of quality and performance.
In this role you will be responsible for:
  • Product Performance Monitoring and Data Automation: Continuously monitor and assess device performance and quality metrics using device performance data maintained on a data platform. Develop scripts, dashboards, and automated workflows to identify trends, anomalies, and deviations from expected performance, and support timely decisions regarding device calibration, maintenance, or additional technical assessment.
  • Algorithm Development and Validation: Develop, implement, and validate analytical algorithms, including machine learning techniques where appropriate, to automate device performance monitoring, support root cause investigations, and generate objective evidence for engineering decisions. Ensure scripts, models, and associated outputs are documented, version controlled, verified, and validated in accordance with applicable quality system expectations.
  • Issue Resolution and Root Cause Investigation: Investigate and resolve device field issues by analyzing product performance data, customer feedback, and failure reports. Define and execute engineering studies and testing to determine root cause and support effective actions to minimize device downtime and customer impact. Collaborate with cross-functional teams to review and support CAPA and NCMR documents.
  • Design and Process Improvement: Collaborate with cross-functional teams, including R&D and manufacturing, to identify and implement design changes and process improvements that enhance device reliability, performance, and manufacturability.
  • Design Changes & Change Control: Support design and process changes for on-market medical devices, including design impact assessments, design documentation updates, requirements and specification updates, verification planning, implementation through change control processes, and assessment of potential impacts to labeling and risk.
  • Documentation and Compliance: Maintain accurate and comprehensive documentation of engineering changes, investigation records, technical reports, test records, risk documentation, and change control documentation. Ensure all activities comply with regulatory requirements and company standards. Collaborate with quality and regulatory to address regulatory requests
  • Cross-Functional Collaboration: Work closely with manufacturing, quality assurance, regulatory affairs, clinical development, medical affairs, sales, suppliers, and other engineering teams to support product lifecycle management and ensure effective implementation of engineering solutions.
  • Other Duties: Perform other duties as assigned

What you'll need (Required):
  • Bachelor's Degree in Engineering or Scientific field with 2 years of experience -OR- Master's Degree or equivalent in Engineering or Scientific field with industry/education internship, senior project, or thesis
  • Proficiency in engineering software, statistical tools, and scripting for data analysis, in particular Python on Databricks or comparable database/data analytics platforms, plus Minitab, and Excel.
  • Experience developing, validating, and maintaining Python scripts or similar automated data pipelines used for monitoring product performance, detecting anomalies, supporting investigations, or informing maintenance and recalibration decisions.
  • Familiarity with machine learning, statistical process monitoring, predictive analytics, or anomaly detection methods applied to engineering or device performance data.
  • Relocation is not provided for this role. Only candidates within a 50-mile radius of Irvine, CA will be considered.

What we look for (Preferred):
  • Experience supporting on-market medical devices, preferably Class III implantable or electromechanical devices.
  • Working knowledge of medical device design controls, change control, CAPA, complaint investigations, and risk management.
  • Familiarity with ISO 13485, ISO 14971, FDA quality management system regulations, and applicable medical device regulatory expectations.
  • Experience developing or executing verification and validation protocols, engineering test methods, and technical reports.
  • Strong written and verbal communication skills with the ability to clearly document technical rationale and present findings to cross-functional stakeholders.
  • Solid problem-solving, organizational, analytical and critical thinking skills
  • Attention to detail and commitment to high quality documentation.
  • Ability to work effectively in a team-oriented, fast-paced, regulated environment while managing multiple priorities.
  • Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $87,000 to $123,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
COVID Vaccination Requirement
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958

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