ZipRecruiter

Log In

1

Validation Engineer Biomedical Jobs in Oceanside, CA

Abbott

Validation Engineer IV

Lakeside, CA · On-site

Validation Engineer IV Location: 3200 Lakeside Drive, Santa Clara, CA 95054 Duration: 6 Months Work ... Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field. * Minimum ...

Abbott

Validation Engineer IV

Lakeside, CA · On-site

$55 - $60/hr

Validation Engineer IV Location: 3200 Lakeside Drive, Santa Clara, CA 95054 Duration: 6 Months Work ... Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field. * Minimum ...

Alphatec Spine

Validation Engineer II

Carlsbad, CA

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing ... Bachelor's or master's degree in biomedical engineering or related field * 2-8 years of experience ...

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing ... Bachelor's or master's degree in biomedical engineering or related field * 2-8 years of experience ...

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing ... Bachelor's or master's degree in biomedical engineering or related field * 2-8 years of experience ...

Apple

Machine Learning Engineer

San Diego, CA · On-site

Bachelors degree in Computer Science, Electrical Engineering, Biomedical Engineering, Statistics ... Experience owning algorithm development from early exploration through validation and integration ...

Apple

Machine Learning Engineer

San Diego, CA · On-site

Bachelors degree in Computer Science, Electrical Engineering, Biomedical Engineering, Statistics ... early exploration through validation and integration Experience developing algorithms for ...

BioLegend

Validation Specialist

San Diego, CA

BioLegend develops world-class, cutting-edge antibodies and reagents for biomedical research ... Support change control, Engineering control, new product and validations (equipment, methods and ...

Apple

Machine Learning Engineer

San Diego, CA · On-site

$139.50K - $258.10K/yr

... validate ML and GenAI-driven algorithms for health sensing applications from concept through ... Engineering, Biomedical Engineering, Statistics, Applied Mathematics, or related field, or ...

Exthymic

Senior Fluidics Engineer

San Diego, CA · On-site

$110.90K - $152.40K/yr

... validation. * Build and execute test protocols for fluidic performance - Author and run ... Bachelor's or advanced degree in Mechanical Engineering, Biomedical Engineering, Chemical ...

Exthymic

Senior Fluidics Engineer

San Diego, CA · On-site

$110.90K - $152.40K/yr

... validation. * Build and execute test protocols for fluidic performance - Author and run ... Bachelor's or advanced degree in Mechanical Engineering, Biomedical Engineering, Chemical ...

next page

Showing results 1-20

People also search for

All JobsValidation Engineer Biomedical JobsValidation Engineer Biomedical Jobs in Oceanside, CA

Validation Engineer Biomedical information

See Oceanside, CA salary details

$23

$53

$80

How much do validation engineer biomedical jobs pay per hour?

As of May 28, 2026, the average hourly pay for validation engineer biomedical in Oceanside, CA is $53.79, according to ZipRecruiter salary data. Most workers in this role earn between $40.77 and $65.38 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Validation Engineer in Biomedical, and why are they important?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What are some typical challenges faced by Validation Engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What does a Validation Engineer do in the biomedical field?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What is the difference between Validation Engineer Biomedical vs Quality Assurance Engineer Biomedical?

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are popular job titles related to Validation Engineer Biomedical jobs in Oceanside, CA? For Validation Engineer Biomedical jobs in Oceanside, CA, the most frequently searched job titles are:
What job categories do people searching Validation Engineer Biomedical jobs in Oceanside, CA look for? The top searched job categories for Validation Engineer Biomedical jobs in Oceanside, CA are:
What cities near Oceanside, CA are hiring for Validation Engineer Biomedical jobs? Cities near Oceanside, CA with the most Validation Engineer Biomedical job openings:
Validation Engineer Biomedical jobs near you

Validation Engineer IV

Abbott

Lakeside, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired today. Applications are no longer accepted.

Abbott rating

8.0

Company rating: 8.0 out of 10

Based on 129 frontline employees who took The Breakroom Quiz

131st of 511 rated manufacturers

Job description

Job Title: Validation Engineer IV
Location: 3200 Lakeside Drive, Santa Clara, CA 95054
Duration: 6 Months
Work Arrangement: 100% Onsite
Position Overview
We are seeking a Senior Test Method Validation Engineer to join our team in Santa Clara, CA. In this role, you will be part of a product development team focused on delivering next generation transcatheter valve technologies to the global healthcare market.
The engineer will support test method development and validation activities, including testing, statistical analysis, and design collaboration to support product development and process improvement initiatives.
Key Responsibilities
  • Lead test method validation protocol development, execution, statistical analysis, and reporting.
  • Contribute to requirements development to influence product design goals.
  • Support test method and model development for product evaluation.
  • Perform testing and data analysis to support design and process development objectives.
  • Under guidance, contribute to design concept generation to meet engineering requirements.
  • Identify potential design or test method issues and perform root cause analysis.
  • Collaborate with internal teams and external vendors to obtain prototype parts and fixtures.
  • Apply knowledge of measurement system analysis, metrology, and Gage R&R.
  • Support development of risk management documentation (DFMEA, UFMEA, PFMEA) as needed.
  • Execute assigned tasks to support overall project and program goals.
  • Gain working knowledge of quality and regulatory requirements including FDA and ISO standards.
  • Ensure compliance with FDA regulations, company policies, operating procedures, and quality processes.
  • Maintain strong collaboration and communication with cross-functional teams, vendors, and stakeholders.
  • Perform other related duties as assigned.
Required Qualifications
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field.
  • Minimum 5+ years of engineering experience in design, testing, manufacturing, or engineering support.
  • Strong analytical and problem-solving abilities with attention to detail.
  • Ability to work independently with structured guidance in a fast-paced environment.
  • Excellent verbal and written communication skills with the ability to communicate effectively across organizational levels.
  • Proven ability to collaborate with cross-functional teams and stakeholders.
  • Strong organizational, prioritization, and follow-up skills.
Preferred Qualifications
  • Experience in medical device or other regulated industries.
  • Experience with SolidWorks or other CAD tools.
  • Familiarity with electronic document control systems such as Windchill.
  • Experience working within cross-functional teams in a geographically distributed, matrixed organization.
Consultants Eligible Benefits Upon Waiting Period:
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
  • Published on 17 Mar 2026, 1:29 AM

What Abbott employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply