Green Card Quality Assurance Auditor Jobs
Quality Assurance Auditor roles qualify for EB-2 and EB-3 green card sponsorship through the PERM labor certification process, which permanently ties your residency to a U.S. employer rather than a temporary visa status. Employers in manufacturing, pharmaceuticals, and regulated industries regularly sponsor foreign professionals for these compliance-driven positions.
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Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.
Position Summary
We have an opportunity for a Quality Assurance Auditor – Analytical Review. This position requires the ability to perform established routine and non-routine Quality Assurance tasks with minimal supervision in support of internal non-commercial clients, external clients and/or commercial processes and projects as assigned.
Shift: Monday- Friday 8:00am-5:00pm
Location: Greenville, NC
100% Onsite
The Role
- Ensure integrity of data through accurate transactions, documentation, and tracking of all cGMP activities
- Provide broad advocacy for the continued improvement of quality standards and the development and maintenance of a quality culture across the organization
- Work to create an environment of open communication, participation and information-sharing within and between teams within Quality Assurance and throughout the facility
- Support the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards
- Ensure compliance to all compendial, internal and client-specific requirements (i.e. SOPs, Quality Agreements, General and Informational Chapters in multiple compendia as applicable)
- Review/approve laboratory reports and COAs
- Review/approve stability reports (LWRs) in SLIM
- Release of Raw Materials in ERP System
- Ensure all work is performed and documented in accordance with approved standard operating procedures, in compliance with cGMPs
- Provide real time support for laboratories
- Other duties as assigned
The Candidate
Minimum Requirements
- Bachelor’s degree in a Life Sciences discipline with at least 3 years of professional experience in the pharmaceutical industry and at least 1 year in a direct QA role
- Associate degree in a Life Sciences discipline with at least 2 years of professional experience in the pharmaceutical industry and at least 2 years in a direct QA role
- Demonstrated ability to perform detailed analytical review of GMP documentation, laboratory data, batch records, protocols, reports, and quality records
- Position requires the capacity to handle and manipulate objects using hands and arms
Why You Should Join Catalent
- Positive and fast-paced working environment focusing on continual improvement and innovation.
- Competitive Paid Time Off plus 8 paid holidays.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement to help you finish your degree or earn a new one.
- Engaging site-based activities such as Music Bingo, Puppy Supply Donation Program, and seasonal events.
- Employee Resource Groups promoting Diversity and Inclusion.
- Green initiatives and community engagement programs including highway clean-up.
- Defined career path with annual performance reviews and growth opportunities.
- WellHub program promoting physical and mental wellness, including onsite fitness center.
- Exclusive discounts through Perkspot from over 900 merchants.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Job Description
Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.
Position Summary
We have an opportunity for a Quality Assurance Auditor – Analytical Review. This position requires the ability to perform established routine and non-routine Quality Assurance tasks with minimal supervision in support of internal non-commercial clients, external clients and/or commercial processes and projects as assigned.
Shift: Monday- Friday 8:00am-5:00pm
Location: Greenville, NC
100% Onsite
The Role
- Ensure integrity of data through accurate transactions, documentation, and tracking of all cGMP activities
- Provide broad advocacy for the continued improvement of quality standards and the development and maintenance of a quality culture across the organization
- Work to create an environment of open communication, participation and information-sharing within and between teams within Quality Assurance and throughout the facility
- Support the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards
- Ensure compliance to all compendial, internal and client-specific requirements (i.e. SOPs, Quality Agreements, General and Informational Chapters in multiple compendia as applicable)
- Review/approve laboratory reports and COAs
- Review/approve stability reports (LWRs) in SLIM
- Release of Raw Materials in ERP System
- Ensure all work is performed and documented in accordance with approved standard operating procedures, in compliance with cGMPs
- Provide real time support for laboratories
- Other duties as assigned
The Candidate
Minimum Requirements
- Bachelor’s degree in a Life Sciences discipline with at least 3 years of professional experience in the pharmaceutical industry and at least 1 year in a direct QA role
- Associate degree in a Life Sciences discipline with at least 2 years of professional experience in the pharmaceutical industry and at least 2 years in a direct QA role
- Demonstrated ability to perform detailed analytical review of GMP documentation, laboratory data, batch records, protocols, reports, and quality records
- Position requires the capacity to handle and manipulate objects using hands and arms
Why You Should Join Catalent
- Positive and fast-paced working environment focusing on continual improvement and innovation.
- Competitive Paid Time Off plus 8 paid holidays.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement to help you finish your degree or earn a new one.
- Engaging site-based activities such as Music Bingo, Puppy Supply Donation Program, and seasonal events.
- Employee Resource Groups promoting Diversity and Inclusion.
- Green initiatives and community engagement programs including highway clean-up.
- Defined career path with annual performance reviews and growth opportunities.
- WellHub program promoting physical and mental wellness, including onsite fitness center.
- Exclusive discounts through Perkspot from over 900 merchants.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
See all Green Card Quality Assurance Auditor Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Green Card Quality Assurance Auditor Jobs.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Quality Assurance Auditor
Translate your credentials into PERM language
Your foreign QA certifications (ISO auditor credentials, Six Sigma, or industry-specific accreditations) must map to the job duties listed in your PERM labor certification. Document each credential with official transcripts and certification bodies before your employer files with DOL.
Target industries with established PERM filing history
Pharmaceutical manufacturers, medical device companies, and aerospace contractors file PERM applications for QA Auditor roles far more consistently than general consumer goods firms. Prioritize employers in FDA-regulated or ISO 9001-certified environments where sponsorship is a standard hiring practice.
Search sponsoring employers through Migrate Mate
Use Migrate Mate to filter Quality Assurance Auditor openings by employers with active green card sponsorship history. This cuts the research time spent cold-applying to companies that have never filed PERM for this occupation.
Clarify EB-2 versus EB-3 eligibility before accepting an offer
If you hold a master's degree in engineering, quality management, or a related field, push your employer to evaluate EB-2 eligibility before defaulting to EB-3. The degree requirement difference affects your priority date and wait time, particularly for applicants from India or China.
Request the prevailing wage determination before signing
Your employer must file a prevailing wage determination with OFLC before starting the PERM recruitment process. Cross-check the wage level assigned against the OFLC Wage Search for your job title and metropolitan area to confirm it accurately reflects your auditor responsibilities.
Understand how PERM recruitment advertising affects your timeline
DOL requires employers to complete a mandatory recruitment period before filing PERM, typically spanning 30 to 180 days depending on the recruitment steps used. Delays in placing required job ads or documenting recruitment results directly push back your I-140 filing date.
Green Card Quality Assurance Auditor: Frequently Asked Questions
Does a Quality Assurance Auditor role qualify for EB-2 or EB-3 green card sponsorship?
Most Quality Assurance Auditor positions qualify for EB-3 sponsorship as skilled workers requiring at least two years of training or experience. If the role requires a master's degree or equivalent in a specialized field such as quality engineering or regulatory compliance, your employer may be able to pursue EB-2 instead. The classification depends on how the employer defines the minimum requirements in the PERM application.
How does green card sponsorship differ from H-1B sponsorship for QA Auditor roles?
Green card sponsorship through PERM leads to permanent residency with no annual renewal cycle, while H-1B visa status requires periodic extensions and is subject to annual cap lottery risk. EB-3 green card sponsorship has no lottery at the filing stage, though wait times vary significantly by country of birth. The PERM process also requires the employer to formally test the labor market, which adds several months before your I-140 petition can be filed.
Which industries are most likely to sponsor Quality Assurance Auditors for a green card?
Pharmaceutical manufacturers, medical device companies, aerospace firms, and food processing operations are among the most consistent sponsors for QA Auditor roles. These industries operate under strict regulatory frameworks from agencies like the FDA and require ongoing auditor headcount. Their compliance obligations make long-term sponsorship commitments more practical than in less regulated sectors.
Where can I find Quality Assurance Auditor jobs with green card sponsorship?
Migrate Mate is built specifically to surface Quality Assurance Auditor roles at employers with employment-based green card sponsorship history. Rather than filtering through general job listings and cold-applying, you can identify employers who have previously filed PERM or I-140 petitions for this occupation, which significantly narrows your search to realistic sponsorship opportunities.
How long does the green card process take for a Quality Assurance Auditor starting from a job offer?
From job offer to green card approval, the process typically spans two to five years for most nationalities. The PERM labor certification and I-140 petition together take roughly one to two years. Applicants from countries with current priority dates, such as most of Europe, Australia, and Canada, can often file for adjustment of status or an immigrant visa soon after I-140 approval, while applicants from India or China face substantially longer waits due to per-country backlogs. USCIS publishes monthly visa bulletin updates that track priority date movement.