Validation Engineer Green Card Jobs
Validation Engineer roles sit squarely in EB-2 and EB-3 territory: employers regularly sponsor foreign professionals through PERM labor certification, covering everything from process validation in pharma and medical devices to software and systems verification. Strong credentials in engineering disciplines with a bachelor's or advanced degree make sponsorship straightforward for qualified candidates.
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Get Access To All JobsABOUT ABBVIE
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
JOB DESCRIPTION
An engineering professional that works with project owners, subject designers/engineers and other project team members to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes etc. in line with project, operations and quality objectives. Level of responsibility and performance is commensurate with grade level. The main objective is to establish evaluation, testing and documentation for risk management, commissioning and validation applying product and regulatory requirements and risk management to result in robust, high quality products. This includes optimizing systems that support the work in and around this area of responsibility.
This position is fully onsite Monday-Friday but may have periods of time that require nights or weekends (approx. quarterly).
Responsibilities
- Work with end-user and project engineer to develop User Requirements Specifications and Functional / Design Specifications for new or modified equipment, facilities, and utilities.
- Support Factory Acceptance Testing in conjunction with Project Engineer to confirm unit is acceptable.
- Identify risk controls, critical elements and traceability of equipment design based on FMEA or other risk assessment.
- Develop and execute commissioning, qualification and validation test protocols to ensure that the unit functions according to specifications.
- Perform minor troubleshooting of issues encountered during commissioning and documentation of unresolved issues.
- Able to support broader aspects of projects at times including: project leadership, developing operational procedures, support training of maintenance/technical staff/operators on new equipment, reviewing new or modified product documentation to ensure compatibility with qualified equipment and implementing changes in equipment parameters or recipes.
- Leads Execution of Risk Management, including periodic review and update per the Validation Master Plan, interface with best practices, establishing team's work practices including overall program, ccRA. Understands risk management principles. Can find and review documentation. Understands controls, impact of change, trace controls, and can estimate ratings using appropriate scale. Timely. Demonstrated success in FMEA authorization/facilitation.
- Qualification as QRM facilitator commensurate with responsibility.
- May supervise contract validation resources in the timely completion of activities in his/her area of responsibility.
QUALIFICATIONS
- Bachelor’s Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 3+ years of significant engineering and/or operational experience.
- Experience in the development of commissioning, qualification, validation and risk management deliverables including specifications and testing protocols that can stand up to regulatory scrutiny.
- Strong interpersonal, communication, and negotiation skills with demonstrated ability to work within a team environment.
- Ability to manage complex projects and multiple projects (5+) simultaneously.
PREFERRED QUALIFICATIONS
- 8 years of overall experience in Manufacturing, Quality or Engineering including 4 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.)
- A technical background in medical devices, pharmaceutical, or Biotechnology industries.
- Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing.
- Process and Cleaning Validation Experience.
- Equipment Qualification (IOQ/PQ).
- Quality System Experience (Veeva, Trackwise, ComplianceWire).
- Statistical Analysis (Minitab or JUMP).
ADDITIONAL INFORMATION
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
-
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
-
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
ABOUT ABBVIE
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
JOB DESCRIPTION
An engineering professional that works with project owners, subject designers/engineers and other project team members to plan, and complete tasks associated with commissioning, qualification and validation of new and modified equipment, facilities, utilities, product, processes etc. in line with project, operations and quality objectives. Level of responsibility and performance is commensurate with grade level. The main objective is to establish evaluation, testing and documentation for risk management, commissioning and validation applying product and regulatory requirements and risk management to result in robust, high quality products. This includes optimizing systems that support the work in and around this area of responsibility.
This position is fully onsite Monday-Friday but may have periods of time that require nights or weekends (approx. quarterly).
Responsibilities
- Work with end-user and project engineer to develop User Requirements Specifications and Functional / Design Specifications for new or modified equipment, facilities, and utilities.
- Support Factory Acceptance Testing in conjunction with Project Engineer to confirm unit is acceptable.
- Identify risk controls, critical elements and traceability of equipment design based on FMEA or other risk assessment.
- Develop and execute commissioning, qualification and validation test protocols to ensure that the unit functions according to specifications.
- Perform minor troubleshooting of issues encountered during commissioning and documentation of unresolved issues.
- Able to support broader aspects of projects at times including: project leadership, developing operational procedures, support training of maintenance/technical staff/operators on new equipment, reviewing new or modified product documentation to ensure compatibility with qualified equipment and implementing changes in equipment parameters or recipes.
- Leads Execution of Risk Management, including periodic review and update per the Validation Master Plan, interface with best practices, establishing team's work practices including overall program, ccRA. Understands risk management principles. Can find and review documentation. Understands controls, impact of change, trace controls, and can estimate ratings using appropriate scale. Timely. Demonstrated success in FMEA authorization/facilitation.
- Qualification as QRM facilitator commensurate with responsibility.
- May supervise contract validation resources in the timely completion of activities in his/her area of responsibility.
QUALIFICATIONS
- Bachelor’s Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 3+ years of significant engineering and/or operational experience.
- Experience in the development of commissioning, qualification, validation and risk management deliverables including specifications and testing protocols that can stand up to regulatory scrutiny.
- Strong interpersonal, communication, and negotiation skills with demonstrated ability to work within a team environment.
- Ability to manage complex projects and multiple projects (5+) simultaneously.
PREFERRED QUALIFICATIONS
- 8 years of overall experience in Manufacturing, Quality or Engineering including 4 major validation subjects (e.g. Computer, Equipment, Cleaning, Process, etc.)
- A technical background in medical devices, pharmaceutical, or Biotechnology industries.
- Knowledge of quality / compliance management as well as regulations and standards affecting API, Bulk Drug or Finished goods manufacturing.
- Process and Cleaning Validation Experience.
- Equipment Qualification (IOQ/PQ).
- Quality System Experience (Veeva, Trackwise, ComplianceWire).
- Statistical Analysis (Minitab or JUMP).
ADDITIONAL INFORMATION
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
-
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
-
This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
See all 350+ Validation Engineer jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Validation Engineer roles.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Validation Engineer
Document your validation methodology credentials
PERM requires proving your qualifications match the job's minimum requirements. Gather transcripts, certifications like CAPA or IQ/OQ/PQ documentation, and employer letters that tie your hands-on validation experience to the specific engineering duties in the role.
Target industries with established PERM pipelines
Pharmaceutical manufacturers, medical device companies, and semiconductor fabs file PERM petitions for Validation Engineers far more regularly than general manufacturers. Filtering by NAICS code 3254 or 3344 in DOL disclosure data surfaces employers with active sponsorship history.
Search green card sponsoring employers on Migrate Mate
Use Migrate Mate to filter Validation Engineer openings by employers with EB-2 or EB-3 green card sponsorship history, so you're applying to companies already familiar with the PERM process rather than educating hiring managers from scratch.
Clarify EB-2 versus EB-3 eligibility before accepting an offer
EB-2 requires a master's degree or a bachelor's plus five years of progressive experience; EB-3 covers roles needing a bachelor's. Ask the sponsoring employer which category they plan to file under, since this affects your priority date and wait time.
Verify prevailing wage before negotiating your salary
Your employer must pay at least the DOL prevailing wage for your specific validation role and work location. Run the OFLC Wage Search before your negotiation so your offered salary meets the Level II or Level III wage floor required for PERM certification.
Confirm the employer's PERM recruitment timeline upfront
PERM requires the employer to run a supervised recruitment campaign before filing. Ask HR whether they've completed a prevailing wage determination and how long their internal legal review typically takes, since total PERM processing at DOL currently runs six to twelve months.
Validation Engineer jobs are hiring across the US. Find yours.
Find Validation Engineer JobsValidation Engineer Green Card Sponsorship: Frequently Asked Questions
Do Validation Engineer jobs commonly qualify for EB-2 or EB-3 green card sponsorship?
Yes. Validation Engineer roles in regulated industries like pharmaceuticals, biotech, and medical devices consistently meet EB-3 requirements because they require at least a bachelor's degree in engineering or a related field. EB-2 applies when the role requires a master's degree or when the candidate holds a bachelor's plus five years of progressive, specialized validation experience. Employers in FDA-regulated environments file PERM petitions for these roles routinely.
How does green card sponsorship differ from H-1B sponsorship for Validation Engineers?
H-1B sponsorship grants temporary status in two or three year increments and is subject to an annual lottery that can delay authorization by a year or more. EB-2 and EB-3 green card sponsorship through PERM leads to permanent residency with no annual lottery and no cap on petitions filed. The tradeoff is time: PERM filing and I-140 approval together take roughly one to two years before you even reach adjustment of status, whereas an approved H-1B lets you start working immediately.
What does PERM labor certification actually require from a Validation Engineer sponsor?
The employer must obtain a prevailing wage determination from DOL, conduct a supervised recruitment campaign to demonstrate no qualified U.S. workers are available, and then file an ETA Form 9089 with OFLC. For Validation Engineer roles, the job description must reflect actual daily duties and not overstate requirements to screen out otherwise qualified applicants. DOL audits these filings, so accuracy in describing validation scope, software tools, and regulatory frameworks matters.
How can I find Validation Engineer jobs where the employer already sponsors green cards?
Migrate Mate lets you search Validation Engineer openings specifically filtered by employers with EB-2 or EB-3 sponsorship history, which saves significant time compared to applying broadly and discovering sponsorship policies during the offer stage. Prioritizing employers with a documented PERM filing history means you're talking to companies whose legal and HR teams already understand the process.
Can I use O*NET to verify that my Validation Engineer role qualifies as a specialty occupation?
O*NET classifies Validation Engineers under industrial and quality engineering occupations, which are recognized as requiring specialized knowledge and at minimum a bachelor's degree in an engineering discipline. Reviewing the O*NET profile for your specific role gives you the standardized job zone classification and typical education requirements, which directly supports both the PERM job description and any EB-2 justification your employer's attorney needs to build the petition.
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