E-3 Visa Electronic Engineer Jobs
Electronic Engineer roles in the U.S. qualify for E-3 visa sponsorship when the position requires a relevant engineering degree and meets the specialty occupation standard. The E-3 has no lottery and no annual cap, so Australian engineers can apply as soon as they secure a job offer from a U.S. employer willing to file an LCA.
Find E-3 Visa Electronic Engineer JobsOverview
Showing 5 of 9+ Electronic Engineer jobs
See all Electronic Engineer Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Electronic Engineer roles.
Get Access To All JobsINTRODUCTION
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.
JOB SUMMARY
We are seeking an Associate Director, electronic Quality Management System (eQMS) to provide quality expertise supporting the development and commercialization of Nurix’s products in compliance with relevant US, EU, and ICH requirements. In this role, you will be responsible for actively managing, developing, implementing, and reporting on Quality Systems, including Deviations, Investigations, CAPAs, Change Controls, Complaints, Quality Metrics, and electronic Quality Management Systems (eQMS). You will serve as a subject matter expert (SME) and strategic partner across Technical Operations, Clinical, Regulatory Affairs, and other cross-functional teams, with overall responsibility for the execution, scalability, and continuous improvement of Nurix’s Quality Management System as the organization grows and matures.
JOB RESPONSIBILITIES
- Manage and maintain processes, SOPs, and workflows for Deviations, Investigations, CAPA, Change Control, Complaints, Quality Metrics, and other core QMS programs.
- Lead or support the implementation, configuration, validation, and optimization of the electronic Quality Management System (eQMS), ensuring phase-appropriate design and scalability.
- Provide hands-on expertise in the day-to-day execution, review, and management of QMS records within the eQMS.
- Partner with internal stakeholders to define data governance, system configuration, user roles, and reporting requirements for quality systems.
- Ensure data integrity, traceability, and compliance of quality system data in accordance with regulatory expectations (e.g., ALCOA+ principles).
- Monitor overall quality system effectiveness, identify gaps or inefficiencies, and drive continuous improvement initiatives.
- Recommend updates to quality policies and procedures and implement process improvements aligned with organizational growth and regulatory readiness.
- Develop, compile, analyze, and present quality metrics and KPIs for routine management review.
- Perform trending and data analysis to identify risks, systemic issues, and opportunities for improvement.
- Create and deliver training programs related to QMS processes, data integrity, and eQMS functionality.
- Support inspection readiness and ensure adherence to cGMPs, regulatory mandates, and internal quality standards.
- Build and maintain strong cross-functional relationships and foster a culture of engagement, transparency, and quality ownership.
- Perform other duties as assigned.
EXPERIENCE AND SKILLS
- Bachelor’s degree in Computer Science, Life Sciences, or a related field, or equivalent relevant experience.
- Demonstrated experience implementing, administering, and improving an eQMS, including system configuration, validation support, and lifecycle management.
- Minimum of 8 years of experience in the pharmaceutical or biotechnology industry, including 6+ years in Quality Systems / Quality Assurance.
- Strong working knowledge of quality system data management, reporting, and data integrity principles.
- First-hand experience managing and reviewing deviations, investigations, CAPAs, and change controls in a regulated environment.
- Experience using validated computerized systems to manage regulated quality records.
- Proven ability to develop and implement enhancements to electronic Quality Systems to improve usability, compliance, and reporting.
- Strong proficiency with Microsoft Office Suite and related business applications.
- Ability to manage multiple priorities in a fast-paced, evolving environment with strong attention to detail.
- Highly organized, self-motivated, and capable of working independently while effectively collaborating cross-functionally.
- Excellent written and verbal communication skills, with the ability to influence and interact effectively at all levels of the organization.
FIT WITH NURIX CULTURE AND VALUES
- Strong team orientation; highly collaborative
- Solutions and results-oriented focus
- Hands-on approach; resourceful and open to diverse points of view
SALARY RANGE
$200,700 - $233,500
LOCATION
Brisbane, CA - Onsite
INTRODUCTION
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.
JOB SUMMARY
We are seeking an Associate Director, electronic Quality Management System (eQMS) to provide quality expertise supporting the development and commercialization of Nurix’s products in compliance with relevant US, EU, and ICH requirements. In this role, you will be responsible for actively managing, developing, implementing, and reporting on Quality Systems, including Deviations, Investigations, CAPAs, Change Controls, Complaints, Quality Metrics, and electronic Quality Management Systems (eQMS). You will serve as a subject matter expert (SME) and strategic partner across Technical Operations, Clinical, Regulatory Affairs, and other cross-functional teams, with overall responsibility for the execution, scalability, and continuous improvement of Nurix’s Quality Management System as the organization grows and matures.
JOB RESPONSIBILITIES
- Manage and maintain processes, SOPs, and workflows for Deviations, Investigations, CAPA, Change Control, Complaints, Quality Metrics, and other core QMS programs.
- Lead or support the implementation, configuration, validation, and optimization of the electronic Quality Management System (eQMS), ensuring phase-appropriate design and scalability.
- Provide hands-on expertise in the day-to-day execution, review, and management of QMS records within the eQMS.
- Partner with internal stakeholders to define data governance, system configuration, user roles, and reporting requirements for quality systems.
- Ensure data integrity, traceability, and compliance of quality system data in accordance with regulatory expectations (e.g., ALCOA+ principles).
- Monitor overall quality system effectiveness, identify gaps or inefficiencies, and drive continuous improvement initiatives.
- Recommend updates to quality policies and procedures and implement process improvements aligned with organizational growth and regulatory readiness.
- Develop, compile, analyze, and present quality metrics and KPIs for routine management review.
- Perform trending and data analysis to identify risks, systemic issues, and opportunities for improvement.
- Create and deliver training programs related to QMS processes, data integrity, and eQMS functionality.
- Support inspection readiness and ensure adherence to cGMPs, regulatory mandates, and internal quality standards.
- Build and maintain strong cross-functional relationships and foster a culture of engagement, transparency, and quality ownership.
- Perform other duties as assigned.
EXPERIENCE AND SKILLS
- Bachelor’s degree in Computer Science, Life Sciences, or a related field, or equivalent relevant experience.
- Demonstrated experience implementing, administering, and improving an eQMS, including system configuration, validation support, and lifecycle management.
- Minimum of 8 years of experience in the pharmaceutical or biotechnology industry, including 6+ years in Quality Systems / Quality Assurance.
- Strong working knowledge of quality system data management, reporting, and data integrity principles.
- First-hand experience managing and reviewing deviations, investigations, CAPAs, and change controls in a regulated environment.
- Experience using validated computerized systems to manage regulated quality records.
- Proven ability to develop and implement enhancements to electronic Quality Systems to improve usability, compliance, and reporting.
- Strong proficiency with Microsoft Office Suite and related business applications.
- Ability to manage multiple priorities in a fast-paced, evolving environment with strong attention to detail.
- Highly organized, self-motivated, and capable of working independently while effectively collaborating cross-functionally.
- Excellent written and verbal communication skills, with the ability to influence and interact effectively at all levels of the organization.
FIT WITH NURIX CULTURE AND VALUES
- Strong team orientation; highly collaborative
- Solutions and results-oriented focus
- Hands-on approach; resourceful and open to diverse points of view
SALARY RANGE
$200,700 - $233,500
LOCATION
Brisbane, CA - Onsite
See all E-3 Visa Electronic Engineer Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new E-3 Visa Electronic Engineer Jobs.
Get Access To All JobsTips for Finding E-3 Visa Sponsorship as an Electronic Engineer
Get your credentials assessed before applying
Australian three-year engineering degrees are generally accepted as equivalent to a U.S. four-year bachelor's degree, but having a formal credential evaluation ready speeds up employer review and removes a common objection during the offer stage.
Target employers with active LCA filing history
Search the DOL's OFLC disclosure data for companies that have filed LCAs for electrical or electronic engineering roles. Employers already familiar with the LCA process move faster and ask fewer questions about E-3 visa sponsorship requirements.
Clarify the specialty occupation link in your resume
Your resume must make it obvious that the role requires a degree in electrical engineering or a directly related field. Generic phrases like 'engineering background' leave room for doubt. Name the specific discipline your degree covers and map it to the job duties.
Address the LCA wage requirement before the offer is finalised
The LCA must certify that your offered wage meets the DOL prevailing wage for the role and location. Confirm with your employer that the salary they're proposing clears this threshold before you accept, so there's no renegotiation after the process starts.
Use Migrate Mate's E-3 filing service to handle your LCA and visa paperwork
Once you have a job offer, Migrate Mate's E-3 filing service manages the LCA submission, DS-160, and consulate preparation end-to-end. Using a dedicated service reduces errors that cause administrative processing delays at the consulate.
Prepare for specialty occupation questions at the consulate
Consular officers can ask you to explain how your engineering degree directly relates to your specific job duties. Bring your offer letter, degree transcripts, and a brief written summary of the technical responsibilities that require your engineering qualification.
E-3 Visa Electronic Engineer: Frequently Asked Questions
How do I find Electronic Engineer jobs with E-3 visa sponsorship?
Migrate Mate is built specifically for Australian professionals searching for U.S. roles with E-3 sponsorship. You can filter by job title and see which employers have a track record of E-3 and LCA filings for engineering roles, so you're not applying blind to companies unfamiliar with the process.
How much does it cost to get an E-3 visa?
Migrate Mate's E-3 filing service covers the entire process for $499, including the Labor Condition Application, visa document preparation, and consulate appointment guidance. Traditional immigration lawyers charge $2,000–$5,000+ for the same work. The E-3 has less paperwork than most work visas, so paying thousands for legal help is usually unnecessary.
Does an Electronic Engineer role qualify as a specialty occupation for the E-3?
Electronic engineering meets the specialty occupation standard when the position genuinely requires a bachelor's degree or higher in electrical engineering, electronics, or a closely related field. Roles where the employer would accept any degree, or where no degree is actually required to perform the work, can fail this test at the consulate.
How does the E-3 compare to the H-1B for Electronic Engineers in the U.S.?
The E-3 has a 10,500 annual allocation that has never been fully used, so there's no lottery and no waiting for a selection round. The H-1B visa is subject to an annual cap and a random lottery, meaning a qualified electronic engineer can wait years for an approved slot. Australian citizens can bypass that entirely with the E-3.
Can I switch employers on an E-3 as an Electronic Engineer?
Yes, but you need to restart the process with the new employer. They must file a fresh LCA with the DOL and you'll need to attend a new consulate appointment to get a new E-3 stamp. You can't transfer an E-3 between employers the way some other visa categories allow a petition transfer.