E-3 Visa Quality Assurance Specialist Jobs
Quality Assurance Specialist roles qualify for E-3 visa sponsorship because they meet the specialty occupation standard, requiring at minimum a bachelor's degree in a relevant field. Australian professionals can secure two-year, renewable E-3 status with no lottery and no annual cap to worry about.
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Get Access To All JobsJob Title: QA Specialist
Location: Redmond, WA (onsite)
Shifts: Days 07:00 till 16:00, Tue to Sat or Sun to Thurs (Please confirm which shifts would be best suited for you during application).
About Us: this is who we are
At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!
The Role: / your challenge, …in our journey
We’re looking for a passionate and curious QA Specialist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a QA Specialist at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team. The QA Specialist role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancing the quality assurance systems. The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below.
What You’ll Do (QA Operations)
- Review executed Manufacturing Batch Records
- Execute compliance walkthrough of the Manufacturing floor and other assigned areas.
- Participate in the training of new or junior staff.
- Partner with Manufacturing to ensure compliance in Manufacturing operations.
- Triage Manufacturing events and support event investigations.
- Review and approve Master Batch Records and other supporting documents.
- Support internal and client audits.
- Execute process performance and product quality monitoring programs.
- Alert senior management of significant quality, compliance, supply, and safety risks.
Qualifications
- Bachelor’s degree in biological or engineering science
- Minimum of 3 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
- Ability to collaborate and communicate cross-functionally.
- Proven attention to detail
- Shifts: Days 07:00 till 16:00, Tue to Sat or Sun to Thurs. Please confirm which shift works best for you.
Why Join Us
- Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
- Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role, Redmond.
- Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
- Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
- A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
Are You Still Curious?
If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Just Evotec Biologics. Let your curiosity guide your career—#BeCurious and explore the endless possibilities at Just Evotec Biologics!
The base pay range for this exempt position at commencement of employment is expected to be $87,000 to $95,000; Base salary offered may vary depending on individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.
Job Title: QA Specialist
Location: Redmond, WA (onsite)
Shifts: Days 07:00 till 16:00, Tue to Sat or Sun to Thurs (Please confirm which shifts would be best suited for you during application).
About Us: this is who we are
At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!
The Role: / your challenge, …in our journey
We’re looking for a passionate and curious QA Specialist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a QA Specialist at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team. The QA Specialist role is responsible for the execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancing the quality assurance systems. The role incumbent works both independently and collaboratively with Manufacturing, Quality and Facilities staff to ensure compliance with cGMPs and internal procedures. The responsibilities of the employee is based on the assigned QA organization as outlined below.
What You’ll Do (QA Operations)
- Review executed Manufacturing Batch Records
- Execute compliance walkthrough of the Manufacturing floor and other assigned areas.
- Participate in the training of new or junior staff.
- Partner with Manufacturing to ensure compliance in Manufacturing operations.
- Triage Manufacturing events and support event investigations.
- Review and approve Master Batch Records and other supporting documents.
- Support internal and client audits.
- Execute process performance and product quality monitoring programs.
- Alert senior management of significant quality, compliance, supply, and safety risks.
Qualifications
- Bachelor’s degree in biological or engineering science
- Minimum of 3 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment.
- Ability to collaborate and communicate cross-functionally.
- Proven attention to detail
- Shifts: Days 07:00 till 16:00, Tue to Sat or Sun to Thurs. Please confirm which shift works best for you.
Why Join Us
- Growth Opportunities: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
- Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role, Redmond.
- Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
- Innovative Projects: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
- A Place for Big Ideas: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
Are You Still Curious?
If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of Just Evotec Biologics. Let your curiosity guide your career—#BeCurious and explore the endless possibilities at Just Evotec Biologics!
The base pay range for this exempt position at commencement of employment is expected to be $87,000 to $95,000; Base salary offered may vary depending on individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.
Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.
See all 64+ E-3 Visa Quality Assurance Specialist Jobs
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Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Quality Assurance Specialist
Translate your Australian credentials for U.S. employers
Australian three-year bachelor's degrees in engineering, science, or a related discipline are accepted as equivalent to U.S. four-year degrees for E-3 visa specialty occupation purposes. Get a credential evaluation from a NACES-approved evaluator before applying.
Target industries with documented QA hiring patterns
Medical device, pharmaceutical, aerospace, and software sectors file LCAs for Quality Assurance Specialists at higher volumes than other industries. Focus your applications on regulated industries where documented QA processes are a compliance requirement, not a preference.
Confirm your job offer specifies a degree requirement
The E-3 specialty occupation standard requires that the role normally needs a bachelor's degree in a specific field. If your offer letter or job description says 'preferred' instead of 'required,' ask the employer to revise it before the LCA is filed.
Use Migrate Mate's E-3 filing service for your LCA and paperwork
The LCA must be certified by DOL before your consulate appointment. Migrate Mate's E-3 filing service manages the entire process from offer to consulate appointment, so you and your employer avoid paperwork errors that delay certification.
Prepare for nonimmigrant intent questions at your interview
QA roles in the U.S. are often long-term positions, which can prompt consular officers to probe your ties to Australia. Bring documentation of property, family connections, or professional memberships in Australia to demonstrate intent to return when your status ends.
Request a new LCA when changing employers or roles
An approved E-3 visa is tied to a specific employer and position. If you're switching companies or moving into a different QA function, your new employer must file a fresh LCA with DOL and you'll need a new visa stamp before re-entering the U.S.
E-3 Visa Quality Assurance Specialist: Frequently Asked Questions
How do I find Quality Assurance Specialist jobs that offer E-3 visa sponsorship?
Migrate Mate is built specifically for this search. It surfaces Quality Assurance Specialist roles where employers have a demonstrated history of sponsoring work visas, so you're not wasting applications on companies unfamiliar with the E-3 process. Filter by role and location to find positions already matched to your visa situation.
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 a Quality Assurance Specialist role qualify as a specialty occupation for the E-3?
Yes, in most cases. The E-3 specialty occupation standard requires that the position normally demands a bachelor's degree or higher in a specific field such as engineering, computer science, chemistry, or a related discipline. QA roles in regulated industries like medical devices, pharmaceuticals, and aerospace consistently meet this threshold. Roles that accept any degree or no degree may not qualify, so the job description wording matters.
How does the E-3 visa compare to the H-1B for Quality Assurance Specialist positions?
For Australian nationals, the E-3 is strictly preferable. The H-1B visa is subject to an annual lottery with roughly a 25% selection rate and a fixed cap of 85,000 slots. The E-3 has a separate annual allocation of 10,500 visas that has never been fully used, so there's no lottery and no cap risk. The employer-side paperwork is also lighter, making sponsorship easier to secure.
Can I change employers while on an E-3 in a QA role?
Yes, but you can't transfer an existing E-3 to a new employer the way an H-1B allows portability. Your new employer must file a fresh Labor Condition Application with DOL, and you'll need a new E-3 visa stamp from an Australian consulate or a U.S. embassy before returning to the U.S. Plan for this lead time before you give notice at your current job.