Lead Scientist Visa Sponsorship Jobs in Maryland
Lead scientist visa sponsorship jobs in Maryland are concentrated around federal research hubs and life sciences employers in the Baltimore-Washington corridor. Institutions such as the National Institutes of Health, Johns Hopkins University, and major biotech firms in Rockville and Gaithersburg regularly sponsor international scientists for specialized research and development roles.
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Get Access To All JobsSenior QC Scientist - Program Management
About Site
Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities, is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.
The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.
The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.
Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.
Position Summary
We have an opportunity for a Senior QC Scientist - Program Management to join our team. This role serves as the key liaison between Quality Control and clients, ensuring testing requirements are met across internal and external laboratories. The position involves close collaboration with Project Management and other internal teams to establish and maintain testing processes. The successful candidate will play a vital role in coordinating activities, maintaining timelines, and ensuring quality standards are upheld.
Shift: Monday – Friday, 8am – 5pm.
Location: Harmans, MD - BWI
100% Onsite
The Role
- Serve as the primary Quality Control (QC) liaison for clients, internal project teams, and outsourced testing laboratories, ensuring alignment on testing requirements, deliverables, and timelines.
- Coordinate QC activities across Project Management, Process Development, Analytical Development, Quality Control, and Quality Assurance to support GMP manufacturing readiness.
- Manage internal and external testing execution, including method transfers, outsourced testing support, and deliverable tracking.
- Partner with QC sample management and critical reagent teams to oversee sample, reagent, and material inventories, shipments, and logistics.
- Establish and coordinate stability programs with clients and internal stability teams.
- Generate, review, and maintain client sampling plans, ensuring accurate sample collection and testing schedules.
- Develop and maintain project trackers, monitoring QC milestones, deliverables, and testing progress for assigned clients.
- Align manufacturing schedules with QC testing activities to ensure timely testing and reporting.
- Communicate QC-related updates, testing results, and project status effectively to clients and internal stakeholders.
- Support a flexible, compliance-focused environment through participation in training, adherence to campaign-specific requirements, and availability for occasional off-hour or weekend activities.
- Perform other duties as assigned by management.
The Candidate
Minimum Requirements
- Bachelor’s degree in Biology, Chemistry, Engineering, Pharmacy, Information Technology, or a related discipline, and 4–8 years of experience working in a Quality Control environment (reduced experience may be considered with higher education in the same field).
- Strong working knowledge of GMP regulations, ICH guidelines, FDA requirements, USP/EP standards, and other applicable U.S. and EU regulatory expectations.
- Proven ability to manage multiple priorities in a fast-paced environment, demonstrating strong organizational skills, responsiveness, sound judgment, and attention to detail.
- Excellent written and verbal communication skills with the ability to effectively collaborate across cross-functional teams, leadership, and external clients.
- Strong analytical and problem-solving capabilities with the ability to assess complex Quality Control issues and drive effective resolutions.
- Proficiency with Microsoft Office Suite (Excel, Word, PowerPoint), Microsoft Project, and Smartsheet.
- Demonstrated ability to apply scientific, quality, and regulatory principles to support operational, compliance, and Quality Control activities.
- Highly detail-oriented with a commitment to accuracy, follow-through, and continuous improvement.
Preferred Skills & Background
- Project Management and Contract Manufacturing experience.
Pay
The anticipated salary range for this position in MD is $110,000 – $120,000 plus bonus. The final salary offered to a successful candidate may vary and will depend on several factors, including but not limited to the type and length of experience within the job, type and length of experience within the industry, skillset, education, and business needs. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
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.
Visit Catalent Careers to explore career opportunities.
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.
Senior QC Scientist - Program Management
About Site
Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The campus, featuring two manufacturing facilities, is located 5 miles from the Baltimore Washington International (BWI) airport and 13 miles from our Baltimore location. The campus is close to Washington, DC’s I-270 Technology Corridor, top universities, and government agencies.
The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse.
The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing.
Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based therapies and vaccines.
Position Summary
We have an opportunity for a Senior QC Scientist - Program Management to join our team. This role serves as the key liaison between Quality Control and clients, ensuring testing requirements are met across internal and external laboratories. The position involves close collaboration with Project Management and other internal teams to establish and maintain testing processes. The successful candidate will play a vital role in coordinating activities, maintaining timelines, and ensuring quality standards are upheld.
Shift: Monday – Friday, 8am – 5pm.
Location: Harmans, MD - BWI
100% Onsite
The Role
- Serve as the primary Quality Control (QC) liaison for clients, internal project teams, and outsourced testing laboratories, ensuring alignment on testing requirements, deliverables, and timelines.
- Coordinate QC activities across Project Management, Process Development, Analytical Development, Quality Control, and Quality Assurance to support GMP manufacturing readiness.
- Manage internal and external testing execution, including method transfers, outsourced testing support, and deliverable tracking.
- Partner with QC sample management and critical reagent teams to oversee sample, reagent, and material inventories, shipments, and logistics.
- Establish and coordinate stability programs with clients and internal stability teams.
- Generate, review, and maintain client sampling plans, ensuring accurate sample collection and testing schedules.
- Develop and maintain project trackers, monitoring QC milestones, deliverables, and testing progress for assigned clients.
- Align manufacturing schedules with QC testing activities to ensure timely testing and reporting.
- Communicate QC-related updates, testing results, and project status effectively to clients and internal stakeholders.
- Support a flexible, compliance-focused environment through participation in training, adherence to campaign-specific requirements, and availability for occasional off-hour or weekend activities.
- Perform other duties as assigned by management.
The Candidate
Minimum Requirements
- Bachelor’s degree in Biology, Chemistry, Engineering, Pharmacy, Information Technology, or a related discipline, and 4–8 years of experience working in a Quality Control environment (reduced experience may be considered with higher education in the same field).
- Strong working knowledge of GMP regulations, ICH guidelines, FDA requirements, USP/EP standards, and other applicable U.S. and EU regulatory expectations.
- Proven ability to manage multiple priorities in a fast-paced environment, demonstrating strong organizational skills, responsiveness, sound judgment, and attention to detail.
- Excellent written and verbal communication skills with the ability to effectively collaborate across cross-functional teams, leadership, and external clients.
- Strong analytical and problem-solving capabilities with the ability to assess complex Quality Control issues and drive effective resolutions.
- Proficiency with Microsoft Office Suite (Excel, Word, PowerPoint), Microsoft Project, and Smartsheet.
- Demonstrated ability to apply scientific, quality, and regulatory principles to support operational, compliance, and Quality Control activities.
- Highly detail-oriented with a commitment to accuracy, follow-through, and continuous improvement.
Preferred Skills & Background
- Project Management and Contract Manufacturing experience.
Pay
The anticipated salary range for this position in MD is $110,000 – $120,000 plus bonus. The final salary offered to a successful candidate may vary and will depend on several factors, including but not limited to the type and length of experience within the job, type and length of experience within the industry, skillset, education, and business needs. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
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.
Visit Catalent Careers to explore career opportunities.
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.
Lead Scientist Job Roles in Maryland
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Search Lead Scientist Jobs in MarylandLead Scientist Jobs in Maryland: Frequently Asked Questions
Which visa types realistically fit lead scientist roles in Maryland?
Lead scientist positions typically qualify as specialty occupations requiring a directly related bachelor's degree or higher, making the H-1B visa the most common sponsorship path. Researchers at universities or nonprofit research institutions may access cap-exempt H-1B petitions. EB-2 and EB-3 employment-based green cards are also pursued by employers seeking permanent hires. J-1 visa exchange visitor status suits postdoctoral and research scholar appointments at designated sponsor organizations. Chilean nationals may qualify under H-1B1 and Singaporean nationals under H-1B1 Singapore, both of which cover specialty occupations.
Which companies sponsor visas for lead scientists in Maryland?
Maryland's dense biotech and federal research presence generates consistent lead scientist sponsorship activity. Major filers include AstraZeneca, Novavax, and Emergent BioSolutions, which maintain large R&D operations in Montgomery County. Johns Hopkins University, the University of Maryland, and federal contractors affiliated with NIH and FDA campuses in Bethesda and Silver Spring also file regularly for research scientists and principal investigators with specialized expertise.
How to find lead scientist visa sponsorship jobs in Maryland?
Migrate Mate lists Maryland employers with verified lead scientist sponsorship history, letting you search by role and location across the Baltimore-Washington corridor. Because sponsorship data is verified through employer filing records, you can prioritize companies that have actively petitioned for scientists rather than those that only indicate openness to it. Filtering to Maryland-specific postings helps focus your search on the biotech clusters in Rockville, Gaithersburg, and the Baltimore metro area.
Which cities in Maryland have the most lead scientist sponsorship jobs?
Rockville and Gaithersburg in Montgomery County account for the highest concentration, anchored by biotech and pharmaceutical companies operating near the NIH campus. Baltimore is a secondary hub driven by Johns Hopkins, the University of Maryland Medical System, and life sciences employers along the I-270 corridor. Bethesda and Silver Spring attract scientists connected to federal health agencies and their affiliated contractors, creating additional sponsorship activity in those communities.
Are there state-specific factors that affect lead scientist visa sponsorship in Maryland?
Maryland's proximity to NIH, FDA, and other federal health agencies creates an unusually strong pipeline for international scientists, with many employers experienced in sponsoring specialty occupation petitions. University and nonprofit research institutions affiliated with these agencies can often file H-1B petitions outside the annual cap, reducing wait time uncertainty. Maryland's BioHealth Capital Region initiative has also attracted multinational life sciences companies that maintain dedicated immigration support infrastructure for research hires.
What is the prevailing wage for sponsored lead scientist jobs in Maryland?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.