UCB H-1B Visa Sponsorship Jobs USA
UCB sponsors H-1B visas for specialized roles across its drug discovery, clinical development, regulatory affairs, and commercial operations teams. The company has a focused sponsorship program that tends to favor candidates with deep scientific or technical expertise in neurology and immunology.
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Get Access To All JobsMake your mark for patients
We are looking for a Regulatory CMC Scientist to join us in our Global Regulatory team, based in any of our Brussels (Belgium), Slough (UK) or Raleigh/Atlanta (US) offices.
About the role
Define the strategy, planning and preparation (writing and review) of CMC submission documentation for regulatory submissions (new marketing applications, variations) from a global/regional perspective to achieve timely approvals to meet business needs.
Who you’ll work with
You will work within the Regulatory CMC team and partner with other technical and regulatory functions across the business.
What you’ll do
- Responsible for regional and global CMC submissions in line with agreed global regulatory strategy, and within agreed timelines.
- Contribute and ensure adequate provision of regulatory CMC input to all Health Authority (HA) interactions on CMC matters in all regions.
- Ensures effective communication of CMC regulatory strategy, risks, and overall plan to GRA Teams, Technical, Development and Commercial Teams.
- Highlights anticipated and ongoing critical issues arising through the product life cycle in a timely manner to senior management to enable communication to key stakeholders.
- Lead or contribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, and evaluation/implementation of digital strategies and tools.
Basic Qualifications
- Bachelor’s degree, Master’s preferred in a relevant life science or business-related discipline.
- Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance CMC and Device regulatory strategy, submission quality, lifecycle management, and decision-making across global markets.
- Significant relevant experience in the pharmaceutical industry preferably in Regulatory Affairs CMC with focus on biological entities.
- Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological entities.
- Knowledge of GMP requirements, standard systems (e.g. change management systems and tools).
- Effective interpersonal, presentation and communication skills with established internal and external stakeholders.
- Proven leadership, problem-solving ability, flexibility, influence, and effective teamwork skills.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Make your mark for patients
We are looking for a Regulatory CMC Scientist to join us in our Global Regulatory team, based in any of our Brussels (Belgium), Slough (UK) or Raleigh/Atlanta (US) offices.
About the role
Define the strategy, planning and preparation (writing and review) of CMC submission documentation for regulatory submissions (new marketing applications, variations) from a global/regional perspective to achieve timely approvals to meet business needs.
Who you’ll work with
You will work within the Regulatory CMC team and partner with other technical and regulatory functions across the business.
What you’ll do
- Responsible for regional and global CMC submissions in line with agreed global regulatory strategy, and within agreed timelines.
- Contribute and ensure adequate provision of regulatory CMC input to all Health Authority (HA) interactions on CMC matters in all regions.
- Ensures effective communication of CMC regulatory strategy, risks, and overall plan to GRA Teams, Technical, Development and Commercial Teams.
- Highlights anticipated and ongoing critical issues arising through the product life cycle in a timely manner to senior management to enable communication to key stakeholders.
- Lead or contribute to ongoing process improvement and department initiatives within the CMC Regulatory Affairs function, including process improvements, SOP review and development, and evaluation/implementation of digital strategies and tools.
Basic Qualifications
- Bachelor’s degree, Master’s preferred in a relevant life science or business-related discipline.
- Demonstrated ability to leverage digital tools, structured data, and regulatory information systems to enhance CMC and Device regulatory strategy, submission quality, lifecycle management, and decision-making across global markets.
- Significant relevant experience in the pharmaceutical industry preferably in Regulatory Affairs CMC with focus on biological entities.
- Proven track record of successful authoring and contribution to delivering CMC sections of marketing authorisations for new biological entities.
- Knowledge of GMP requirements, standard systems (e.g. change management systems and tools).
- Effective interpersonal, presentation and communication skills with established internal and external stakeholders.
- Proven leadership, problem-solving ability, flexibility, influence, and effective teamwork skills.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Job Roles at UCB
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Get Access To All JobsTips for Finding UCB H-1B Jobs
Target UCB's core therapeutic areas
UCB concentrates its pipeline in neurology and immunology. Candidates with research, clinical, or regulatory backgrounds in these areas are far more likely to receive H-1B sponsorship than those applying to generalist or administrative roles.
Verify sponsorship history before applying
Not every UCB role comes with H-1B sponsorship. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and avoid wasting applications on positions that don't support international candidates.
Understand UCB's H-1B filing calendar
UCB must file H-1B petitions with USCIS before the April lottery cap deadline. Timing your application and offer acceptance well before that window closes is critical to securing sponsorship for the October start date.
Lead with your specialty occupation credentials
UCB's H-1B sponsorship depends on demonstrating your role qualifies as a specialty occupation. Highlight your degree field's direct relevance to the position in your resume and interviews to strengthen the petition case.
Engage UCB's talent acquisition team early
In biotechnology and pharmaceuticals, H-1B sponsorship decisions often involve HR, legal, and hiring managers together. Raising your visa status early in conversations allows UCB to loop in the right people before an offer is extended.
Pursue roles in R&D, regulatory, and medical affairs
UCB's H-1B sponsorship activity is concentrated in scientific and technical functions. Roles in drug development, pharmacovigilance, biostatistics, and medical affairs consistently align with the specialty occupation standard H-1B petitions require.
UCB H-1B Visa Sponsorship: Frequently Asked Questions
Does UCB sponsor H-1B visas?
Yes, UCB sponsors H-1B visas for qualified candidates in specialized scientific and technical roles. Sponsorship is most common in areas like clinical development, regulatory affairs, research, and medical affairs, where the specialty occupation requirement is clearly met. UCB also accepts F-1 OPT and TN visa holders, giving international candidates multiple pathways to get started.
Which departments at UCB are most likely to offer H-1B sponsorship?
UCB's H-1B sponsorship tends to concentrate in its core scientific and technical functions, including drug discovery research, clinical operations, regulatory affairs, biostatistics, pharmacovigilance, and medical affairs. These departments align closely with the specialty occupation standard that H-1B petitions require. General business or administrative roles are less commonly sponsored.
How do I apply for a job at UCB that includes H-1B sponsorship?
Start by identifying UCB roles that explicitly mention visa sponsorship or fall within its core biotechnology functions. Migrate Mate can help you filter for UCB positions with confirmed H-1B sponsorship history. Once you apply, be transparent about your immigration status early in the interview process so UCB's HR and legal teams can assess sponsorship feasibility before an offer is made.
How do I know if my UCB job offer will include H-1B sponsorship?
H-1B sponsorship at UCB is not automatic with every job offer. It depends on the role's qualification as a specialty occupation and UCB's internal sponsorship policies at the time of hiring. Ask directly during the offer stage whether the position includes H-1B support, and clarify which steps UCB handles internally versus through outside immigration counsel.
What timeline should I expect for H-1B sponsorship at UCB?
The H-1B process follows USCIS's annual cycle: lottery registration opens in March, cap-subject petitions are filed in April, and employment typically begins October 1. UCB will need to file a Labor Condition Application with the Department of Labor before submitting your petition. Build in enough lead time to complete onboarding and gather documentation well before the April filing deadline.
What is the prevailing wage for H-1B jobs at UCB?
H-1B employers must pay at least the prevailing wage, which is determined when they file the Labor Condition Application with the Department of Labor. The rate is based on the role, location, and experience level, and ensures international hires are paid comparably to U.S. workers in the same position. You can look up prevailing wage rates for any occupation and location using the DOL's OFLC Wage Search tool.