Software Quality Engineer Visa Sponsorship Jobs in Maryland
Software quality engineer visa sponsorship jobs in Maryland are concentrated around the Baltimore metro, Rockville, and the Washington D.C. corridor, where federal contractors like Lockheed Martin, Leidos, and Booz Allen Hamilton maintain large engineering teams. The state's defense, cybersecurity, and biotech sectors create steady demand for QA engineering talent with specialized technical backgrounds.
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Get Access To All JobsJob Description:
The Manufacturing Execution System (MES) Quality Engineer II position will work closely with the IT, Operations, Validation, and Engineering teams to ensure that projects (new MES deployments, sustaining, and/or optimization) related to MES are implemented compliantly and in a timely manner. This role will support production to drive continuous improvement. The position will also ensure compliance to quality policy, develop requirements, revise/create procedures, develop validation test cases, and maintain the integrity of the electronic device history record (eDHR).
Roles & Responsibilities:
- Act as an integrated MES team member to support new MES deployments, sustaining, and optimization projects.
- Demonstrates understanding and application of engineering principles on cross-functional projects.
- Develop and/or revise MES requirements documentation, procedures, control plans, PFMEAs, and training materials.
- Maintain the compliance of the MES, the integrity of its validated state, and the eDHR.
- Proactively identifies requirements gaps, investigates, and implements best-in-class Quality Engineering practices and solutions.
- Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues related to MES.
- Develop MES validation test cases and support Software Verification & Validation activities.
- Support the Elkton, MD site as a subject matter expert (SME) related to MES and the integration with Product Life Cycle Management.
- Develop training strategy plans and support MES team to deliver training on MES processes.
- May need to work across shifts during some phases of MES deployments.
- Perform other job-related duties.
Background Experience:
Requires Bachelor's degree (4 years) or higher from an accredited course of study, in engineering, engineering technology, computer science or technical field with relevant experience. Requires at least three (3) years experiences in a medical device or highly regulated industry. Experience working in a manufacturing environment preferred. Experience with implementing and maintaining a Manufacturing Execution System / eDHR preferred. Experience with Change Management, Computer System Validation, and Client ALM preferred.
Knowledge, Skills and Abilities (KSAs):
- Knowledge of national and international regulations applicable to medical devices including Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485, and MDD 93/42/EEC.
- Excellent communication skills; verbal and written.
- Ability to work as a team member on cross-functional teams and with employees across all levels within the facility.
- Excellent computer skills and working knowledge of Microsoft Office Suite.
- Problem-solving and critical thinking.
- Detail and results oriented.
- Self-motivated and driven.
- Ability to multitask, prioritize, and provide deliverables within the required timeframe.
- Excellent organizational and time management skills.
Job Description:
The Manufacturing Execution System (MES) Quality Engineer II position will work closely with the IT, Operations, Validation, and Engineering teams to ensure that projects (new MES deployments, sustaining, and/or optimization) related to MES are implemented compliantly and in a timely manner. This role will support production to drive continuous improvement. The position will also ensure compliance to quality policy, develop requirements, revise/create procedures, develop validation test cases, and maintain the integrity of the electronic device history record (eDHR).
Roles & Responsibilities:
- Act as an integrated MES team member to support new MES deployments, sustaining, and optimization projects.
- Demonstrates understanding and application of engineering principles on cross-functional projects.
- Develop and/or revise MES requirements documentation, procedures, control plans, PFMEAs, and training materials.
- Maintain the compliance of the MES, the integrity of its validated state, and the eDHR.
- Proactively identifies requirements gaps, investigates, and implements best-in-class Quality Engineering practices and solutions.
- Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues related to MES.
- Develop MES validation test cases and support Software Verification & Validation activities.
- Support the Elkton, MD site as a subject matter expert (SME) related to MES and the integration with Product Life Cycle Management.
- Develop training strategy plans and support MES team to deliver training on MES processes.
- May need to work across shifts during some phases of MES deployments.
- Perform other job-related duties.
Background Experience:
Requires Bachelor's degree (4 years) or higher from an accredited course of study, in engineering, engineering technology, computer science or technical field with relevant experience. Requires at least three (3) years experiences in a medical device or highly regulated industry. Experience working in a manufacturing environment preferred. Experience with implementing and maintaining a Manufacturing Execution System / eDHR preferred. Experience with Change Management, Computer System Validation, and Client ALM preferred.
Knowledge, Skills and Abilities (KSAs):
- Knowledge of national and international regulations applicable to medical devices including Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485, and MDD 93/42/EEC.
- Excellent communication skills; verbal and written.
- Ability to work as a team member on cross-functional teams and with employees across all levels within the facility.
- Excellent computer skills and working knowledge of Microsoft Office Suite.
- Problem-solving and critical thinking.
- Detail and results oriented.
- Self-motivated and driven.
- Ability to multitask, prioritize, and provide deliverables within the required timeframe.
- Excellent organizational and time management skills.
Software Quality Engineer Job Roles in Maryland
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Search Software Quality Engineer Jobs in MarylandSoftware Quality Engineer Jobs in Maryland: Frequently Asked Questions
Which companies sponsor visas for software quality engineers in Maryland?
Federal contractors and technology firms are the most active sponsors for software quality engineers in Maryland. Companies such as Leidos, Northrop Grumman, Booz Allen Hamilton, and Lockheed Martin regularly hire QA engineering roles and have established visa sponsorship programs. Biotech and life sciences firms in the I-270 corridor, including those supporting FDA regulatory work, also sponsor software quality engineers with relevant domain experience.
Which visa types are most common for software quality engineers in Maryland?
The H-1B is the most common visa for software quality engineers in Maryland, as the role consistently qualifies as a specialty occupation requiring at least a bachelor's degree in computer science, software engineering, or a related field. Some candidates with advanced credentials pursue O-1A classification. Professionals from Canada and Mexico may be eligible for TN status under the 'Computer Systems Analyst' category, depending on the specific job duties.
Which cities in Maryland have the most software quality engineer sponsorship jobs?
Baltimore and its surrounding suburbs account for a large share of software quality engineer sponsorship activity, particularly in defense technology and healthcare IT. Rockville, Bethesda, and Gaithersburg along the I-270 technology corridor are also significant hubs, driven by federal agencies, biotech firms, and government contractors. Columbia and Annapolis occasionally post QA engineering roles tied to cybersecurity and financial services.
How to find software quality engineer visa sponsorship jobs in Maryland?
Migrate Mate is built specifically to surface visa sponsorship jobs for international candidates, including software quality engineer roles in Maryland. You can filter directly by state and role to see positions from employers with active sponsorship histories. This saves time compared to manually screening postings, since Migrate Mate focuses exclusively on employers willing to sponsor work visas rather than listing all open positions regardless of sponsorship intent.
Are there state-specific considerations for software quality engineers seeking sponsorship in Maryland?
Maryland's high concentration of federal contractors introduces one important consideration: many QA engineering roles require security clearances, and clearance eligibility is generally restricted to U.S. citizens and permanent residents. International candidates on work visas should prioritize roles at commercial technology, biotech, or healthcare IT firms, which typically do not carry clearance requirements. The University of Maryland and Johns Hopkins also feed strong local hiring pipelines that occasionally include sponsorship-eligible positions.
What is the prevailing wage for sponsored software quality engineer jobs in Maryland?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.
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