Biotech & Pharma Jobs in Washington DC with TN Sponsorship
TN visa sponsorship jobs in biotech and pharma are available in Washington DC, where federal agencies, research institutions, and life sciences contractors create steady demand for Canadian and Mexican professionals. Organizations like the NIH, FDA, and contractors supporting government health initiatives regularly hire in roles that qualify under TN specialty occupation categories.
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Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Summary:
The Senior Manager, 340B Program Integrity leads enterprise 340B program integrity efforts including validating claims flagged for potential duplicate discounts, identifying diversion activities, and managing Good Faith Inquiries (GFIs) and audits in coordination with vendor partners. This position is responsible for ensuring program integrity efforts are executed in a compliant and timely manner and align with the enterprise 340B strategy.
Responsibilities:
- Review and validate Medicaid claims flagged for potential duplicate discounts
- Analyze chargeback data to identify potential diversion activities
- Lead GFI and audit processes including identification and prioritization of CEs, compiling supporting data, securing necessary internal reviews and approvals, and engaging CEs in collaboration with Legal and external vendors
- Select and manage vendors for GFI support and audits in partnership with the Senior Director, Business Optimization & Analytics Lead
- Ensure all program integrity activities align with HRSA rules and regulations and internal compliance policies and procedures
- Collaborate with the Senior Director, 340B Business Optimization & Analytics Lead to provide feedback on analytics and tools used to support duplicate discount and diversion activity identification
- Document and report GFI and audit metrics, outcomes, and trends to the 340B COE leadership team and executives
- Identify and recommend process improvements to strengthen program integrity efforts
Qualifications
- Bachelor's degree required; advanced degree or certification in compliance, health administration, or business preferred
- 4-6 years of experience in compliance, audit management, or government pricing, ideally within a pharmaceutical or healthcare environment
- Skilled in managing complex, cross-functional projects within a matrixed organization
- Proven ability to analyze complex data sets and identify trends and insights
- Excellent organizational and communication skills with strong attention to detail and documentation accuracy
- Experience selecting and managing vendors
- Strong knowledge of 340B program requirements, including manufacturer GFI and audit rules and procedures
- Prior experience managing 340B program integrity activities including GFIs and audits within a pharmaceutical manufacturer
LI-Hybrid
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Princeton - NJ - US: $139,200 - $168,683
Washington DC - US: $139,200 - $168,683
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
- Health Coverage: Medical, pharmacy, dental, and vision care.
- Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
- Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
- US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
- Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science™, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1599846: Senior Manager, 340B Program Integrity

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Summary:
The Senior Manager, 340B Program Integrity leads enterprise 340B program integrity efforts including validating claims flagged for potential duplicate discounts, identifying diversion activities, and managing Good Faith Inquiries (GFIs) and audits in coordination with vendor partners. This position is responsible for ensuring program integrity efforts are executed in a compliant and timely manner and align with the enterprise 340B strategy.
Responsibilities:
- Review and validate Medicaid claims flagged for potential duplicate discounts
- Analyze chargeback data to identify potential diversion activities
- Lead GFI and audit processes including identification and prioritization of CEs, compiling supporting data, securing necessary internal reviews and approvals, and engaging CEs in collaboration with Legal and external vendors
- Select and manage vendors for GFI support and audits in partnership with the Senior Director, Business Optimization & Analytics Lead
- Ensure all program integrity activities align with HRSA rules and regulations and internal compliance policies and procedures
- Collaborate with the Senior Director, 340B Business Optimization & Analytics Lead to provide feedback on analytics and tools used to support duplicate discount and diversion activity identification
- Document and report GFI and audit metrics, outcomes, and trends to the 340B COE leadership team and executives
- Identify and recommend process improvements to strengthen program integrity efforts
Qualifications
- Bachelor's degree required; advanced degree or certification in compliance, health administration, or business preferred
- 4-6 years of experience in compliance, audit management, or government pricing, ideally within a pharmaceutical or healthcare environment
- Skilled in managing complex, cross-functional projects within a matrixed organization
- Proven ability to analyze complex data sets and identify trends and insights
- Excellent organizational and communication skills with strong attention to detail and documentation accuracy
- Experience selecting and managing vendors
- Strong knowledge of 340B program requirements, including manufacturer GFI and audit rules and procedures
- Prior experience managing 340B program integrity activities including GFIs and audits within a pharmaceutical manufacturer
LI-Hybrid
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Princeton - NJ - US: $139,200 - $168,683
Washington DC - US: $139,200 - $168,683
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
- Health Coverage: Medical, pharmacy, dental, and vision care.
- Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
- Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include:
Paid Time Off
- US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
- Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science™, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1599846: Senior Manager, 340B Program Integrity
Job Roles in Biotech & Pharma in Washington DC
See all 109+ Biotech & Pharma Washington DC jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Biotech & Pharma Washington DC roles.
Get Access To All JobsFrequently Asked Questions
Which biotech and pharma companies sponsor TN visas in Washington DC?
Washington DC's biotech and pharma hiring is anchored by federal contractors and research-focused organizations. Employers like Booz Allen Hamilton, Leidos, SAIC, and ICF work closely with agencies such as the NIH and FDA and have historically hired in life sciences roles. Smaller CROs and biotech consultancies operating near the DC metro area also support TN sponsorship for qualified Canadian and Mexican professionals.
Which areas in Washington DC have the most biotech and pharma TN sponsorship jobs?
Most biotech and pharma TN sponsorship activity in the DC area is concentrated in the broader National Capital Region rather than the District itself. Rockville and Gaithersburg in Montgomery County, Maryland, are particularly active, hosting a dense cluster of life sciences firms and NIH-adjacent contractors. Northern Virginia, including Bethesda and Tysons, also sees consistent hiring in pharma and health sciences roles.
What types of biotech and pharma roles typically qualify for TN sponsorship?
TN visa eligibility in biotech and pharma generally applies to roles requiring a specific bachelor's degree or higher in a relevant scientific or technical field. Positions such as biochemist, microbiologist, pharmacist, medical technologist, and scientific or regulatory affairs specialist commonly qualify. The role must align with a recognized TN occupation category, and the employer must confirm the position requires the applicable specialty degree.
How do I find biotech & pharma TN sponsorship jobs in Washington DC?
Migrate Mate is built specifically for TN visa holders and lists biotech and pharma jobs in Washington DC that include TN sponsorship. Rather than filtering through general job boards and guessing at sponsorship willingness, Migrate Mate surfaces roles where employers have indicated openness to TN candidates, saving time for Canadian and Mexican professionals actively searching in the DC life sciences market.
Are there any DC-specific considerations for TN sponsorship in biotech and pharma?
Washington DC's biotech and pharma sector has an unusually high proportion of roles tied to federal government contracts, which can affect TN sponsorship. Security clearance requirements attached to some contractor positions may complicate or limit eligibility for non-US citizens. Additionally, regulatory affairs roles supporting the FDA require candidates to demonstrate that their degree and job duties align precisely with a qualifying TN occupation category.
See which biotech & pharma employers are hiring and sponsoring visas in Washington DC right now.
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