J-1 Visa Quality Analyst Jobs
Quality Analyst roles in the United States are accessible to exchange visitors through J-1 visa sponsorship, most commonly under the Trainee or Intern program categories. Designated sponsor organizations issue your DS-2019 and oversee your training plan, while your U.S. host employer provides the hands-on quality assurance experience.
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Get Access To All JobsWho We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
SUMMARY
The BioMarin Summer Internship Program will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin, while gaining an insight into the pharmaceutical/biotech industry. Over the course of 10 - 12 weeks our interns gain industry experience while working alongside our talented team on meaningful projects. This role is in our Manufacturing department.
JOB DESCRIPTION/PROJECT:
We are seeking a motivated Manufacturing Operations Analyst intern to support 5S and inspection readiness activities within our Drug Substance Facility. This role offers hands-on experience to GMP manufacturing, continuous improvement, and regulatory compliance in a biotech environment. The intern will partner closely with Manufacturing, Quality, and Engineering teams to help ensure workspaces, documentation, and visual management tools meet inspection-ready standards.
Required Skills:
- Strong organizational and attention to detail skills
- Ability to work independently and manage multiple tasks
- Comfortable working in a regulated environment
- Proficiency in Microsoft Office (Excel, Word, PowerPoint)
Desired Skills:
- Familiarity with 5S, Lean, or Six Sigma concepts
- Interest in manufacturing, operations excellence, or quality
- Strong communication and documentation skills
Qualifications/Eligibility:
- Student currently pursuing a Bachelor’s degree in: Engineering (Chemical, Bioengineering, Industrial), Biotechnology, Life Sciences, Operations, or related field
- Work performed in an active manufacturing environment
- Will require gowning and adherence to GMP Procedures
- Standing and walking in manufacturing areas required
- Must be available to work full time, 40 hours a week.
- Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program.
- Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles. Some positions will be open to remote interns, but employee must be within United States borders.
Benefits of a BioMarin Internship:
- Paid hourly wage, paid company holidays, and sick time
- Apply skills and knowledge learned in the classroom to on-the-job experiences
- Comprehensive, value-added project(s)
- Develop skills specific to your major.
- Opportunities for professional development by building relationships and learning about other parts of the business.
- Participate in company all hands meetings, monthly community lunches
- Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
- Access to Employee Resource Groups
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
In the U.S., the salary range for this position is $24 to $27 per hour, which factors in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors.
Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities. Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we’ve produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
About Technical Operations
BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
SUMMARY
The BioMarin Summer Internship Program will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin, while gaining an insight into the pharmaceutical/biotech industry. Over the course of 10 - 12 weeks our interns gain industry experience while working alongside our talented team on meaningful projects. This role is in our Manufacturing department.
JOB DESCRIPTION/PROJECT:
We are seeking a motivated Manufacturing Operations Analyst intern to support 5S and inspection readiness activities within our Drug Substance Facility. This role offers hands-on experience to GMP manufacturing, continuous improvement, and regulatory compliance in a biotech environment. The intern will partner closely with Manufacturing, Quality, and Engineering teams to help ensure workspaces, documentation, and visual management tools meet inspection-ready standards.
Required Skills:
- Strong organizational and attention to detail skills
- Ability to work independently and manage multiple tasks
- Comfortable working in a regulated environment
- Proficiency in Microsoft Office (Excel, Word, PowerPoint)
Desired Skills:
- Familiarity with 5S, Lean, or Six Sigma concepts
- Interest in manufacturing, operations excellence, or quality
- Strong communication and documentation skills
Qualifications/Eligibility:
- Student currently pursuing a Bachelor’s degree in: Engineering (Chemical, Bioengineering, Industrial), Biotechnology, Life Sciences, Operations, or related field
- Work performed in an active manufacturing environment
- Will require gowning and adherence to GMP Procedures
- Standing and walking in manufacturing areas required
- Must be available to work full time, 40 hours a week.
- Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program.
- Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles. Some positions will be open to remote interns, but employee must be within United States borders.
Benefits of a BioMarin Internship:
- Paid hourly wage, paid company holidays, and sick time
- Apply skills and knowledge learned in the classroom to on-the-job experiences
- Comprehensive, value-added project(s)
- Develop skills specific to your major.
- Opportunities for professional development by building relationships and learning about other parts of the business.
- Participate in company all hands meetings, monthly community lunches
- Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
- Access to Employee Resource Groups
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
In the U.S., the salary range for this position is $24 to $27 per hour, which factors in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors.
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Get Access To All JobsTips for Finding J-1 Visa Sponsorship as a Quality Analyst
Frame your credentials around training objectives
J-1 Trainee sponsors require a structured training plan tied to your field of study or prior work. Document your quality assurance coursework, ISO standards exposure, or quality management certifications before approaching a designated sponsor.
Distinguish Intern from Trainee eligibility early
If you're currently enrolled in a degree program, the Intern category applies. If you've graduated within the past 12 months or have at least one year of relevant quality or inspection experience abroad, Trainee is your category.
Search Migrate Mate to find host employers open to J-1 quality roles
Many U.S. manufacturers and inspection firms hire quality analysts without advertising J-1 compatibility. Migrate Mate filters roles by visa type so you can identify host employers already familiar with the J-1 exchange visitor structure.
Target industries with established J-1 host track records
Automotive, aerospace, medical device, and pharmaceutical manufacturers regularly host J-1 trainees in quality functions. These sectors have internal compliance teams that understand DOL training plan requirements and OFLC wage expectations for technical roles.
Verify your training plan covers measurable quality competencies
Your designated sponsor reviews the DS-7002 training plan for specificity. Outline concrete quality deliverables like defect rate analysis, process audits, or SPC implementation rather than vague tasks. Sponsors reject plans that read as ordinary employment.
Clarify the two-year home residency requirement before accepting an offer
Some J-1 participants are subject to a two-year home-country residency requirement after program completion, depending on government funding or skills list status. Confirm your situation with your designated sponsor before signing a host employer offer letter.
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Find Quality Analyst JobsQuality Analyst J-1 Visa: Frequently Asked Questions
Which J-1 program category fits a Quality Analyst role?
Most Quality Analyst participants enter under the Trainee category, which applies to foreign nationals with a degree plus one year of relevant experience, or five years of professional experience in quality assurance. Current students completing a degree may qualify under the Intern category if the placement relates directly to their field of study.
Who actually sponsors my J-1 visa for a quality analyst position?
Your visa sponsor is a U.S. Department of State-designated organization such as Cultural Vistas or AIPT, not your host employer. The designated sponsor issues your DS-2019 form, signs your training plan, and monitors your program compliance. Your host employer provides the quality assurance work experience but does not control visa sponsorship status.
How do I find U.S. employers willing to host J-1 quality analysts?
Migrate Mate lets you search for roles and employers that align with J-1 exchange visitor programs, including quality and inspection positions. Many host employers in manufacturing and regulated industries understand the J-1 structure but don't label job postings accordingly, so filtering by visa type surfaces opportunities that generic job searches miss.
Can a Quality Analyst J-1 trainee work on a production floor or only in an office?
Your authorized activities are defined by the DS-7002 training plan, not a blanket rule. A training plan that includes production audits, in-line inspection, or statistical process control activities on the floor is valid as long as your designated sponsor approves it. Work that falls entirely outside the approved plan is a compliance violation regardless of setting.
Does the two-year home residency requirement apply to quality analyst trainees?
It depends on your funding source and your home country's skills shortage list. If your J-1 program is funded by your home government or the U.S. government, or if your occupation appears on the Exchange Visitor Skills List for your country, the two-year requirement applies. Your designated sponsor can confirm your status before your DS-2019 is issued.
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