Green Card Quality Assurance Engineer Jobs
Quality Assurance Engineer roles qualify for EB-2 and EB-3 green card sponsorship through PERM labor certification, which requires your employer to document the hiring process before filing your I-140 petition. PERM ties the sponsorship to a specific role and employer, so identifying companies with active green card filing history is the most direct path to permanent residency.
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This Supplier Quality Assurance Engineer III will be based out of one of Omnicell's US Manufacturing Facility - located in Cranberry Township, PA. This is a senior position with high visibility and impact. This role’s primary function is to ensure quality standards are implemented and effective throughout Omnicell’s international Manufacturing and Service supply base with an additional focus on New Product Introductions. This SQ department member will work closely with Global Supply Chain, Manufacturing Engineering personnel at Omnicell to understand current product quality issues and assist with root cause and corrective action with suppliers.
Responsibilities:
- Lead Supplier Design for Manufacturability discussions with support from internal engineering teams.
- Manage supplier qualifications for both NPI and sustaining engineering changes.
- Lead in the development of Supplier IQ/OQ/PQ Protocols and Final Reports, ensuring sampling sizes are statistically valid.
- Guide suppliers to establish and maintain controlled manufacturing processes utilizing Control Plans, PFMEA’s, and Statistical Process Control.
- Lead SCAR activities for supplier product and process quality issues, ensuring all facets of CAPA activities are addressed including effectiveness.
- Plan and execute supplier audits to ensure performance to Omnicell quality standards and regulatory requirements are being met.
- Data collection, analysis, and trending of supplier performance data from ERP system and PLM database.
- Creation of metric reports and presentations for Internal, Supplier QBRs and Management Review.
- Develop, communicate & implement strategies for improving performance of Omnicell’s Manufacturing & Service suppliers.
- Work closely with other QA departments within the Omnicell Global Factory Network on assigning and monitoring effectiveness of Supplier Corrective Actions in a timely manner.
Additional Responsibilities:
- Act as a change agent who accepts and supports new ideas and processes.
- Commitment to cost reduction/controls.
- Lead the ongoing maintenance and continual improvement of Supplier Quality processes.
- Update/creation of internal procedures as required.
- Participate in corporate quality improvement projects as required.
Required Knowledge and Skills:
- Proven working knowledge of auditing methodologies associated with ISO 9001 and ISO 13485 standards.
- Quality concepts/tools (Pareto, fishbone diagram, FMEA, etc.).
- Proficient understanding of engineering and manufacturing terminology and processes such as sheet metal forming, injection molding, die casting, PCB manufacturing, SMT, Thermoforming, Reaction Molding.
- Self-starter with the ability to own projects and tasks to ensure timely execution from start to finish.
- Excellent comprehension of engineering drawings and specifications.
- Proactive, self-motivated, and empathetic work ethic in a fast-paced work environment.
- Ability to effectively interface and communicate with multiple constituents, including senior management, suppliers, consultants, and employees of all levels.
- Ability to work collaboratively with peers and team members.
- Strongly demonstrated written and verbal communication and presentation skills to all levels of an organization.
- Refined multi-tasking and time management skills.
- Ability to consistently balance sense of urgency with diplomacy/empathy.
- Ability to make decisions and execute directives.
- Strongly demonstrated attention to detail.
- Strongly demonstrated organizational and project management skills.
- Demonstrated proficiency with common MS office programs (Word, Excel, PowerPoint, Project).
- Ability to work under tight deadlines and handle multiple detail-oriented projects.
Basic Qualifications:
- Minimum (5) years quality/manufacturing experience
- BS Degree in Engineering or Technical Science
- ISO 13485 or FDA regulated medical device experience
Preferred Qualifications:
- ISO 13485 and ISO 9001 Certified Lead Auditor from accredited body
- ISO 9001, ISO 14001, 21CFR820 experience
- Six-Sigma Green Belt or higher
- Demonstrated knowledge in sheet metal forming and/or injection molding
Work Conditions:
- Office Environment
- May travel up to 30% (including international)
EEO, Privacy, and Adaptability
Omnicell welcomes applications from all individuals, valuing a wide range of perspectives and backgrounds. As an equal opportunity employer, we do not discriminate based on race, gender, religion, sexual orientation, gender identity, national origin, veteran status, or disability. We are committed to making our recruitment process accessible to everyone. We offer support and reasonable adjustments for individuals with disabilities during our hiring process. If you need assistance, please contact us at Recruiting@omnicell.com.
At Omnicell, respect for privacy and confidentiality is paramount. We adhere to strict policies to prevent discrimination or retaliation against those who engage in open conversations about compensation. However, employees privy to compensation information as part of their job role are expected to maintain confidentiality, except in specific circumstances outlined by law, such as during formal complaints, investigations, or as required by legal obligations. Learn more about our privacy practices: https://www.omnicell.com/privacy/
Please note that Omnicell reserves the right to modify job roles and responsibilities as needed to meet our organization's evolving needs and drive our mission forward.
About Us
At Omnicell, innovation starts with people who are passionate about making healthcare safer and smarter. Since 1992, we’ve been transforming the future of pharmacy care through bold ideas and hands-on solutions that make a real impact on clinicians and patients’ lives.
We build outcomes-driven technology—from robotics to intelligent software—that helps clinicians work more efficiently and ensures patients get the care they need. Every improvement, every breakthrough, every idea is rooted in our belief that better is always possible.
But what sets us apart isn’t just the work we do, it’s how we do it. Our Culture of Care shapes everything, from how we show up for each other to how we solve tough problems together. You’ll find a team that has your back, leaders who listen, and a shared commitment to building something that matters.
Here, careers are more than job titles, they are journeys of purpose and possibility. Whether you’re just getting started or ready to grow in new directions, we’ll meet you where you are, with support, flexibility, and opportunity that matches your ambition.
If you’re driven by purpose and ready to shape what’s next in healthcare, there’s a place for you at Omnicell.
Description
This Supplier Quality Assurance Engineer III will be based out of one of Omnicell's US Manufacturing Facility - located in Cranberry Township, PA. This is a senior position with high visibility and impact. This role’s primary function is to ensure quality standards are implemented and effective throughout Omnicell’s international Manufacturing and Service supply base with an additional focus on New Product Introductions. This SQ department member will work closely with Global Supply Chain, Manufacturing Engineering personnel at Omnicell to understand current product quality issues and assist with root cause and corrective action with suppliers.
Responsibilities:
- Lead Supplier Design for Manufacturability discussions with support from internal engineering teams.
- Manage supplier qualifications for both NPI and sustaining engineering changes.
- Lead in the development of Supplier IQ/OQ/PQ Protocols and Final Reports, ensuring sampling sizes are statistically valid.
- Guide suppliers to establish and maintain controlled manufacturing processes utilizing Control Plans, PFMEA’s, and Statistical Process Control.
- Lead SCAR activities for supplier product and process quality issues, ensuring all facets of CAPA activities are addressed including effectiveness.
- Plan and execute supplier audits to ensure performance to Omnicell quality standards and regulatory requirements are being met.
- Data collection, analysis, and trending of supplier performance data from ERP system and PLM database.
- Creation of metric reports and presentations for Internal, Supplier QBRs and Management Review.
- Develop, communicate & implement strategies for improving performance of Omnicell’s Manufacturing & Service suppliers.
- Work closely with other QA departments within the Omnicell Global Factory Network on assigning and monitoring effectiveness of Supplier Corrective Actions in a timely manner.
Additional Responsibilities:
- Act as a change agent who accepts and supports new ideas and processes.
- Commitment to cost reduction/controls.
- Lead the ongoing maintenance and continual improvement of Supplier Quality processes.
- Update/creation of internal procedures as required.
- Participate in corporate quality improvement projects as required.
Required Knowledge and Skills:
- Proven working knowledge of auditing methodologies associated with ISO 9001 and ISO 13485 standards.
- Quality concepts/tools (Pareto, fishbone diagram, FMEA, etc.).
- Proficient understanding of engineering and manufacturing terminology and processes such as sheet metal forming, injection molding, die casting, PCB manufacturing, SMT, Thermoforming, Reaction Molding.
- Self-starter with the ability to own projects and tasks to ensure timely execution from start to finish.
- Excellent comprehension of engineering drawings and specifications.
- Proactive, self-motivated, and empathetic work ethic in a fast-paced work environment.
- Ability to effectively interface and communicate with multiple constituents, including senior management, suppliers, consultants, and employees of all levels.
- Ability to work collaboratively with peers and team members.
- Strongly demonstrated written and verbal communication and presentation skills to all levels of an organization.
- Refined multi-tasking and time management skills.
- Ability to consistently balance sense of urgency with diplomacy/empathy.
- Ability to make decisions and execute directives.
- Strongly demonstrated attention to detail.
- Strongly demonstrated organizational and project management skills.
- Demonstrated proficiency with common MS office programs (Word, Excel, PowerPoint, Project).
- Ability to work under tight deadlines and handle multiple detail-oriented projects.
Basic Qualifications:
- Minimum (5) years quality/manufacturing experience
- BS Degree in Engineering or Technical Science
- ISO 13485 or FDA regulated medical device experience
Preferred Qualifications:
- ISO 13485 and ISO 9001 Certified Lead Auditor from accredited body
- ISO 9001, ISO 14001, 21CFR820 experience
- Six-Sigma Green Belt or higher
- Demonstrated knowledge in sheet metal forming and/or injection molding
Work Conditions:
- Office Environment
- May travel up to 30% (including international)
EEO, Privacy, and Adaptability
Omnicell welcomes applications from all individuals, valuing a wide range of perspectives and backgrounds. As an equal opportunity employer, we do not discriminate based on race, gender, religion, sexual orientation, gender identity, national origin, veteran status, or disability. We are committed to making our recruitment process accessible to everyone. We offer support and reasonable adjustments for individuals with disabilities during our hiring process. If you need assistance, please contact us at Recruiting@omnicell.com.
At Omnicell, respect for privacy and confidentiality is paramount. We adhere to strict policies to prevent discrimination or retaliation against those who engage in open conversations about compensation. However, employees privy to compensation information as part of their job role are expected to maintain confidentiality, except in specific circumstances outlined by law, such as during formal complaints, investigations, or as required by legal obligations. Learn more about our privacy practices: https://www.omnicell.com/privacy/
Please note that Omnicell reserves the right to modify job roles and responsibilities as needed to meet our organization's evolving needs and drive our mission forward.
About Us
At Omnicell, innovation starts with people who are passionate about making healthcare safer and smarter. Since 1992, we’ve been transforming the future of pharmacy care through bold ideas and hands-on solutions that make a real impact on clinicians and patients’ lives.
We build outcomes-driven technology—from robotics to intelligent software—that helps clinicians work more efficiently and ensures patients get the care they need. Every improvement, every breakthrough, every idea is rooted in our belief that better is always possible.
But what sets us apart isn’t just the work we do, it’s how we do it. Our Culture of Care shapes everything, from how we show up for each other to how we solve tough problems together. You’ll find a team that has your back, leaders who listen, and a shared commitment to building something that matters.
Here, careers are more than job titles, they are journeys of purpose and possibility. Whether you’re just getting started or ready to grow in new directions, we’ll meet you where you are, with support, flexibility, and opportunity that matches your ambition.
If you’re driven by purpose and ready to shape what’s next in healthcare, there’s a place for you at Omnicell.
See all 3,798+ Green Card Quality Assurance Engineer Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Green Card Quality Assurance Engineer Jobs.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Quality Assurance Engineer
Document your QA credentials before applying
PERM requires your employer to prove no qualified U.S. worker is available for your specific role. Having your degree evaluations, testing certifications, and QA methodology experience clearly documented speeds up that process and reduces the risk of audit delays.
Search Migrate Mate to find QA employers with green card history
Use Migrate Mate to filter Quality Assurance Engineer roles by employers who have previously filed green card petitions. That filing history signals the employer already understands PERM timelines and has internal HR or legal infrastructure to sponsor you.
Target EB-3 roles if your degree is in an adjacent field
QA Engineer positions often accept computer science, industrial engineering, or electrical engineering degrees. EB-3 covers professionals whose degree field isn't an exact match, so don't rule out postings that list a preferred discipline different from yours.
Verify prevailing wage using the OFLC Wage Search
Before accepting an offer tied to green card sponsorship, check the OFLC Wage Search for your job title and work location. Your employer's PERM filing must certify your offered salary meets the prevailing wage, and mismatches are a common cause of certification delays.
Confirm your employer uses E-Verify before your PERM starts
PERM filings are submitted through the DOL FLAG system, and employers who haven't navigated government labor portals before sometimes underestimate the setup time. Ask your HR contact whether the company uses E-Verify and has filed PERM applications previously.
Negotiate your job title to match the PERM description exactly
USCIS scrutinizes whether your actual duties match the role described in the PERM application. If your offer letter calls you a QA Engineer but your work includes senior-level responsibilities, the petition can face a Request for Evidence. Align your title and duties before the application is filed.
Green Card Quality Assurance Engineer: Frequently Asked Questions
Do Quality Assurance Engineer roles qualify for both EB-2 and EB-3 green card categories?
Yes. QA Engineer positions typically qualify under EB-3 when the role requires a bachelor's degree in engineering, computer science, or a related field. If the role requires an advanced degree or the candidate holds a master's or higher with strong professional credentials, EB-2 may apply. Your employer's PERM filing will specify which category is appropriate based on the minimum job requirements.
How does PERM green card sponsorship differ from H-1B sponsorship for QA Engineers?
H-1B visa is a temporary status with a three-year initial period and an annual lottery cap that creates real uncertainty. PERM-based green card sponsorship has no lottery and leads to permanent residency. The tradeoff is timeline: PERM labor certification, I-140 approval, and adjustment of status typically take two to four years or longer for some nationalities. The outcome, however, is permanent authorization rather than a visa you must continuously renew.
What does the PERM labor certification process look like for a QA Engineer role?
Your employer files a PERM application with the DOL certifying they conducted a good-faith recruitment effort and found no qualified, available U.S. worker for your specific QA Engineer position. The recruitment must follow strict DOL requirements, including advertising the role at the prevailing wage. Once DOL certifies the PERM, your employer files the I-140 immigrant petition with USCIS, and you proceed to adjustment of status or consular processing.
How do I find QA Engineer jobs where the employer is already prepared to sponsor a green card?
Migrate Mate is the most direct way to search Quality Assurance Engineer roles filtered by employers with verified green card filing history. An employer who has previously sponsored PERM petitions already has legal counsel, HR workflows, and budget allocated for immigration, which significantly reduces the risk that your sponsorship stalls due to internal inexperience.
Can my employer start PERM sponsorship while I'm on H-1B or OPT status?
Yes. PERM labor certification is not tied to your current visa status. Employers routinely initiate the green card process for QA Engineers who are already working on H-1B. If you're on OPT, an employer can begin PERM at any time, though the I-485 adjustment of status cannot be filed until a visa number is available for your category and country of birth.