KBI Biopharma Visa Sponsorship USA
KBI Biopharma is a contract development and manufacturing organization (CDMO) known for supporting both early-stage and commercial biopharmaceutical programs. The company sponsors multiple visa types, including H-1B and Green Cards, making it a meaningful option for international scientists and researchers building careers in U.S. biotech.
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INTRODUCTION
At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.
Position Summary
The Electronic Laboratory Notebook (ELN) Administrator position is responsible for supporting the ELN system within the Analytical Formulation Sciences (AFS) Department at KBI. This position is responsible for providing timely end user support/guidance/assistance in the ELN system, as well as building, modifying, and maintaining templates and other user-managed information, conducting user training for the system, and providing basic troubleshooting. Additionally, this position is a technical lead/subject-matter-expert for the ELN system, responsible for coordinating and collaborating with AFS department management, the ELN Product Owner, and IT on system improvement initiatives, system maintenance, as well as the implementation of system configuration updates and new releases. This position is also responsible to support client audits and regulatory inspections as needed.
Responsibilities:
- Provide technical and end user support to ensure efficient and trouble-free operation of the ELN system.
- Configure, deploy, and manage IDBS ELN templates and other user-managed information for efficient data recording and retrieval.
- Maintain a strong working relationship with internal AFS customers, other KBI site AFS departments, the ELN Product Owner, and IT to facilitate the implementation of new releases, configuration updates, or addition of new features, ensuring enhanced functionality and user experience based on business needs.
- Serve as the voice of customer for AFS ELN users, receiving and disseminating end-user feedback regarding the system to AFS management, the Product Owner and IT.
- Lead and/or participate in system improvement initiatives.
- Train team members on ELN usage and best practices.
- Perform data analysis to extract meaningful insights from the ELN.
- Support client/regulatory audits as necessary.
REQUIREMENTS:
- Bachelor’s degree in computer science, pharmaceutical science, biology, chemistry, or other related science/IT.
- Minimum of seven years of experience working in the pharmaceutical industry.
- Must have experience and proficiency working within an electronic laboratory notebook system, preferably IDBS, in the pharmaceutical industry.
- Requires knowledge and understanding of common analytical laboratory processes and assays (e.g., chromatography, rDNA, etc.), as well as quality control measures in the laboratory.
- Must have intermediate proficiency, at a minimum, in word processing (preferably Microsoft Word), spreadsheets (preferably Microsoft Excel), PowerPoint, and email.
- Skilled at breaking down complex procedures and assays, pinpointing critical steps and variables, and converting them into consistent, well-structured templates that support clarity and reproducibility.
- Requires previous work in a regulated environment (FDA, EPA, etc.).
- Skilled at conveying information clearly and concisely, both orally and in writing.
- Experience communicating professionally, effectively, and efficiently with all levels of management, cross-functional teams, and external vendors.
- Strong ability to define problems clearly, gather and analyze data, establish factual findings, and draw sound conclusions. Skilled in troubleshooting issues and developing effective, practical solutions. Understands the impact of non-compliant results and maintains strong attention to detail. Able to interpret a wide range of technical instructions and prioritize tasks based on complexity and urgency.
- While performing the duties of this job, the employee is frequently required to sit, to use hands to perform routine activities (i.e., typing, writing, etc.), and to talk and hear. The employee is occasionally required to stand or walk and to reach with hands and arms. The vision requirements include close vision and distance vision.
SALARY RANGE:
- Salary Range: $84,000 - $115,500
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.
ABOUT KBI:
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe.
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds – regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status – and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its workforce. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

INTRODUCTION
At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.
Position Summary
The Electronic Laboratory Notebook (ELN) Administrator position is responsible for supporting the ELN system within the Analytical Formulation Sciences (AFS) Department at KBI. This position is responsible for providing timely end user support/guidance/assistance in the ELN system, as well as building, modifying, and maintaining templates and other user-managed information, conducting user training for the system, and providing basic troubleshooting. Additionally, this position is a technical lead/subject-matter-expert for the ELN system, responsible for coordinating and collaborating with AFS department management, the ELN Product Owner, and IT on system improvement initiatives, system maintenance, as well as the implementation of system configuration updates and new releases. This position is also responsible to support client audits and regulatory inspections as needed.
Responsibilities:
- Provide technical and end user support to ensure efficient and trouble-free operation of the ELN system.
- Configure, deploy, and manage IDBS ELN templates and other user-managed information for efficient data recording and retrieval.
- Maintain a strong working relationship with internal AFS customers, other KBI site AFS departments, the ELN Product Owner, and IT to facilitate the implementation of new releases, configuration updates, or addition of new features, ensuring enhanced functionality and user experience based on business needs.
- Serve as the voice of customer for AFS ELN users, receiving and disseminating end-user feedback regarding the system to AFS management, the Product Owner and IT.
- Lead and/or participate in system improvement initiatives.
- Train team members on ELN usage and best practices.
- Perform data analysis to extract meaningful insights from the ELN.
- Support client/regulatory audits as necessary.
REQUIREMENTS:
- Bachelor’s degree in computer science, pharmaceutical science, biology, chemistry, or other related science/IT.
- Minimum of seven years of experience working in the pharmaceutical industry.
- Must have experience and proficiency working within an electronic laboratory notebook system, preferably IDBS, in the pharmaceutical industry.
- Requires knowledge and understanding of common analytical laboratory processes and assays (e.g., chromatography, rDNA, etc.), as well as quality control measures in the laboratory.
- Must have intermediate proficiency, at a minimum, in word processing (preferably Microsoft Word), spreadsheets (preferably Microsoft Excel), PowerPoint, and email.
- Skilled at breaking down complex procedures and assays, pinpointing critical steps and variables, and converting them into consistent, well-structured templates that support clarity and reproducibility.
- Requires previous work in a regulated environment (FDA, EPA, etc.).
- Skilled at conveying information clearly and concisely, both orally and in writing.
- Experience communicating professionally, effectively, and efficiently with all levels of management, cross-functional teams, and external vendors.
- Strong ability to define problems clearly, gather and analyze data, establish factual findings, and draw sound conclusions. Skilled in troubleshooting issues and developing effective, practical solutions. Understands the impact of non-compliant results and maintains strong attention to detail. Able to interpret a wide range of technical instructions and prioritize tasks based on complexity and urgency.
- While performing the duties of this job, the employee is frequently required to sit, to use hands to perform routine activities (i.e., typing, writing, etc.), and to talk and hear. The employee is occasionally required to stand or walk and to reach with hands and arms. The vision requirements include close vision and distance vision.
SALARY RANGE:
- Salary Range: $84,000 - $115,500
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.
ABOUT KBI:
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe.
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds – regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status – and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its workforce. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.
Job Roles at KBI Biopharma Companies
How to Get Visa Sponsorship in KBI Biopharma Visa Sponsorship USA
Target roles aligned with biopharmaceutical development
KBI Biopharma's sponsorship activity centers on scientific and technical functions. Focus your applications on roles in process development, analytical sciences, quality, and manufacturing, these departments align most closely with the company's CDMO business and sponsorship history.
Highlight your degree field, not just your job title
H-1B eligibility at a biotech CDMO depends heavily on degree-to-role alignment. Emphasize your specific scientific discipline, chemistry, biology, biochemical engineering, in your application materials to strengthen your specialty occupation case from the start.
Consider KBI if you're on OPT and want a Green Card path
KBI Biopharma's track record includes consistent Green Card sponsorship through EB-2 and EB-3, which matters if you're on OPT and planning long-term. Companies with active immigrant visa sponsorship reduce the risk of hitting a dead end after your H-1B years.
Apply early if you're approaching OPT or CPT deadlines
CDMOs like KBI often run structured hiring timelines tied to project pipelines. Starting your outreach three to four months before your work authorization deadline gives the company room to initiate LCA and H-1B filings without rushing the process.
Use Migrate Mate to confirm KBI's sponsorship before applying
Sponsorship willingness isn't always clear from a job listing. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, confirming that KBI Biopharma actively supports international candidates before you invest time in the application.
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Get Access To All JobsFrequently Asked Questions
Does KBI Biopharma sponsor H-1B visas?
Yes, KBI Biopharma sponsors H-1B visas. The company has an active sponsorship track record across both nonimmigrant and immigrant visa categories. Roles in scientific and technical functions, such as process development, quality assurance, and analytical sciences, are most commonly associated with H-1B sponsorship given their specialty occupation requirements.
Which visa types does KBI Biopharma sponsor?
KBI Biopharma sponsors a range of visa types including H-1B, TN, F-1 OPT, and F-1 CPT for nonimmigrant work authorization. On the immigrant side, the company has sponsored Green Cards through EB-2 and EB-3 pathways. This breadth makes KBI a viable option for international candidates at different stages of their U.S. immigration journey.
Which departments at KBI Biopharma are most likely to sponsor visas?
As a contract development and manufacturing organization, KBI Biopharma's core scientific functions drive the majority of its sponsorship activity. Roles in process development, analytical chemistry, bioassay, quality control, and manufacturing sciences are most likely to qualify for H-1B sponsorship due to their specific degree requirements. Regulatory affairs and project management positions may also be eligible depending on the role structure.
How do I find open roles at KBI Biopharma that offer visa sponsorship?
The most reliable approach is to use Migrate Mate, which lists KBI Biopharma as a verified sponsor and surfaces open roles filtered by sponsorship history. This removes the guesswork of identifying which listings actually support international candidates. Once you've identified a role, confirm sponsorship eligibility directly with KBI's recruiter early in the process to avoid surprises later.
How do I time my application to KBI Biopharma around H-1B filing deadlines?
H-1B cap-subject petitions must be filed in April for an October 1 start date, which means your job offer and employer registration typically need to be in place by March. If you're on OPT, aim to have an offer from KBI finalized by January or February at the latest. CDMOs like KBI often have defined hiring cycles, so earlier outreach significantly improves your chances of getting an offer in time for the H-1B window.
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