Replimune Visa Sponsorship USA
Replimune is a clinical-stage biotechnology company pioneering oncolytic immunotherapy treatments for cancer. For international job seekers, it offers a meaningful sponsorship pathway, supporting both temporary work visas and permanent residence routes for specialized roles in a highly technical field.
See All Replimune JobsOverview
Showing 5 of 24+ Replimune Visa Sponsorship USA jobs


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?
See all 24+ Replimune Visa Sponsorship USA jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Replimune Visa Sponsorship USA roles.
Get Access To All Jobs
INTRODUCTION
Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. We imagine a world where cancer is a curable disease. At Replimune, we live by our values: United: We Collaborate for a Common Goal. Audacious: We Are Bold and Innovative. Dedicated: We Give Our Full Commitment. Candid: We Are Honest With Each Other. People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to contribute to the meaningful work we do which could impact the lives of patients. Join us, as we reshape the future.
JOB SUMMARY
A self-motivated, detail-oriented Principal II Associate to join the External Quality team. The successful candidate will assist with the implementation of GxP practices, Quality processes with specific emphasis on Final Drug product disposition at Contract Labeling and 3PL facilities, Product Complaint Handling, and CMO labeling review. This role will require adaptability and eagerness to learn about all aspects of the External Quality processes to support relationships with internal stakeholders, contract manufacturing organizations (CMOs), suppliers, 3PL (third party logistics suppliers) and clinical trial sites. The candidate will also interact cross-functionally with internal Quality Assurance, Quality Control, Clinical Operations, and Regulatory teams to ensure compliance to GxP processes and regulations. This position reports to the Vice President Framingham Site Quality and it requires a depth of understanding and significant experience in GxP, quality, communication skills and business acumen to conduct responsibilities autonomously. The Principal II Associate of External Quality is responsible for providing support to ensure continuous supply of investigational medicinal products and/or commercial products with GxP relevant international regulations (e.g., CFR part 210, 211, ICH6, EU, MHRA) and other global requirements. This position is based in our Framingham location and typically has a 5-day on-site expectation.
Responsibilities
We are looking for someone with strong commercial product complaint experience.
Key responsibilities:
- Review packaging master batch records, packaging, labeling, for investigational medicinal product.
- Managing Product Complaints for Commercial product a must have.
- Assist with conducting investigations ensuring effective root cause analysis and assigning of appropriate CAPAs.
- Maintain required knowledge of applicable regulations and government, industry, and company standards and their interpretations by participating in industry trainings, workshops, and discussion groups.
- Support of other QA projects as needed.
- Minimal Travel required - domestic and international.
- Represents External Quality on inter-departmental and cross-functional teams, ensuring the flow of information and providing Quality guidance.
- Supports continuous improvement by updating policies and procedures as required.
- Collaborates cross functionally to support of Replimune’s overall success.
OTHER RESPONSIBILITIES
- As assigned
QUALIFICATIONS
Education:
- Bachelor's Degree in appropriate Science (chemistry, biology, biochemistry, microbiology), or Engineering discipline required. MSc or PhD preferred.
Required Experience:
- Minimum 6+ years of experience in GCP, GMP, and Quality Assurance/Compliance in the pharmaceutical, biopharma/biologics industry performing direct hands-on work in Quality Assurance, Quality Control, laboratories, manufacturing, supply chain, facilities, or engineering.
- A working knowledge of GxP practices, US FDA and EU GMP regulations and ICH guidelines.
- Demonstrated knowledge and direct experience with Quality Systems and GxP compliance within a regulated environment.
- Experience managing product complaints is preferred.
- Experience managing quality events (i.e. Deviations, CAPA).
- Experience with Master Control, Veeva or eQMS systems preferred.
- Excel, PowerPoint, Word, SmartSheets proficient.
- Experience revising procedures and documents.
- Excellent attention to detail.
- Excellent verbal and written communication and presentation skills across all levels.
- Prioritize and manage multiple priorities and projects with little assistance.
- Familiarity with clinical and commercial supply areas and processes.
ABOUT REPLIMUNE
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options.
SALARY RANGE
Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $127,500.00 - $165,000.00. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer. At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing equity grants subject to Board approval. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.
We are an Equal Opportunity Employer.

INTRODUCTION
Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it. We imagine a world where cancer is a curable disease. At Replimune, we live by our values: United: We Collaborate for a Common Goal. Audacious: We Are Bold and Innovative. Dedicated: We Give Our Full Commitment. Candid: We Are Honest With Each Other. People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, an innovative and collaborative culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to contribute to the meaningful work we do which could impact the lives of patients. Join us, as we reshape the future.
JOB SUMMARY
A self-motivated, detail-oriented Principal II Associate to join the External Quality team. The successful candidate will assist with the implementation of GxP practices, Quality processes with specific emphasis on Final Drug product disposition at Contract Labeling and 3PL facilities, Product Complaint Handling, and CMO labeling review. This role will require adaptability and eagerness to learn about all aspects of the External Quality processes to support relationships with internal stakeholders, contract manufacturing organizations (CMOs), suppliers, 3PL (third party logistics suppliers) and clinical trial sites. The candidate will also interact cross-functionally with internal Quality Assurance, Quality Control, Clinical Operations, and Regulatory teams to ensure compliance to GxP processes and regulations. This position reports to the Vice President Framingham Site Quality and it requires a depth of understanding and significant experience in GxP, quality, communication skills and business acumen to conduct responsibilities autonomously. The Principal II Associate of External Quality is responsible for providing support to ensure continuous supply of investigational medicinal products and/or commercial products with GxP relevant international regulations (e.g., CFR part 210, 211, ICH6, EU, MHRA) and other global requirements. This position is based in our Framingham location and typically has a 5-day on-site expectation.
Responsibilities
We are looking for someone with strong commercial product complaint experience.
Key responsibilities:
- Review packaging master batch records, packaging, labeling, for investigational medicinal product.
- Managing Product Complaints for Commercial product a must have.
- Assist with conducting investigations ensuring effective root cause analysis and assigning of appropriate CAPAs.
- Maintain required knowledge of applicable regulations and government, industry, and company standards and their interpretations by participating in industry trainings, workshops, and discussion groups.
- Support of other QA projects as needed.
- Minimal Travel required - domestic and international.
- Represents External Quality on inter-departmental and cross-functional teams, ensuring the flow of information and providing Quality guidance.
- Supports continuous improvement by updating policies and procedures as required.
- Collaborates cross functionally to support of Replimune’s overall success.
OTHER RESPONSIBILITIES
- As assigned
QUALIFICATIONS
Education:
- Bachelor's Degree in appropriate Science (chemistry, biology, biochemistry, microbiology), or Engineering discipline required. MSc or PhD preferred.
Required Experience:
- Minimum 6+ years of experience in GCP, GMP, and Quality Assurance/Compliance in the pharmaceutical, biopharma/biologics industry performing direct hands-on work in Quality Assurance, Quality Control, laboratories, manufacturing, supply chain, facilities, or engineering.
- A working knowledge of GxP practices, US FDA and EU GMP regulations and ICH guidelines.
- Demonstrated knowledge and direct experience with Quality Systems and GxP compliance within a regulated environment.
- Experience managing product complaints is preferred.
- Experience managing quality events (i.e. Deviations, CAPA).
- Experience with Master Control, Veeva or eQMS systems preferred.
- Excel, PowerPoint, Word, SmartSheets proficient.
- Experience revising procedures and documents.
- Excellent attention to detail.
- Excellent verbal and written communication and presentation skills across all levels.
- Prioritize and manage multiple priorities and projects with little assistance.
- Familiarity with clinical and commercial supply areas and processes.
ABOUT REPLIMUNE
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options.
SALARY RANGE
Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $127,500.00 - $165,000.00. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer. At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing equity grants subject to Board approval. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.
We are an Equal Opportunity Employer.
Job Roles at Replimune Companies
How to Get Visa Sponsorship in Replimune Visa Sponsorship USA
Target scientific and clinical roles first
Replimune's sponsorship activity is concentrated in specialized biotechnology functions, think research, clinical development, and regulatory affairs. Focus your applications on roles where your technical credentials in oncology or immunotherapy are directly relevant to the company's pipeline work.
Understand Replimune's Green Card commitment
Replimune has a track record of sponsoring permanent residence, not just temporary work visas. If long-term U.S. settlement is your goal, this signals genuine investment in retaining international talent beyond an initial visa period.
Know which visa types they support before applying
Replimune sponsors H-1B visas and supports EB-2 and EB-3 Green Card pathways, plus TN visas for eligible Canadian and Mexican nationals. Understanding which category fits your background lets you frame your application around the right sponsorship route from the start.
Demonstrate specialty occupation credentials clearly
H-1B approval at a biotech company depends on establishing that your role requires a highly specialized degree. Highlight your advanced education in a relevant life sciences or clinical field throughout your resume and cover letter to strengthen the specialty occupation case.
Timing matters in biotech hiring cycles
Clinical-stage biotechs like Replimune often hire in bursts tied to trial milestones and funding rounds. Monitor their pipeline announcements and search for open roles on Migrate Mate, which surfaces verified sponsors so you can filter by real sponsorship history.
Replimune jobs are hiring across the US. Find yours.
Find Replimune JobsSee all 24+ Replimune jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Replimune roles.
Get Access To All JobsFrequently Asked Questions
Does Replimune sponsor H-1B visas?
Yes, Replimune sponsors H-1B visas for qualifying roles. As a clinical-stage biotechnology company, it employs professionals in highly specialized scientific and clinical functions that typically meet the specialty occupation standard required for H-1B approval. If your background is in life sciences, oncology research, regulatory affairs, or a related technical discipline, you may be a strong candidate for H-1B sponsorship at Replimune.
What visa types does Replimune sponsor?
Replimune sponsors H-1B visas for temporary work authorization, EB-2 and EB-3 immigrant visa categories for permanent residence, and TN visas for eligible Canadian and Mexican nationals. The combination of temporary and permanent pathways makes Replimune a meaningful option for international candidates who want both a near-term work visa and a long-term route to a U.S. Green Card.
Which departments or roles at Replimune are most likely to receive visa sponsorship?
Sponsorship at Replimune tends to align with the company's core focus areas, oncolytic immunotherapy research, clinical operations, regulatory affairs, bioinformatics, and translational medicine. Roles requiring advanced degrees in molecular biology, oncology, pharmacology, or clinical development are the strongest candidates. Corporate and administrative positions are less commonly sponsored, though it varies by role and business need.
How do I find open roles at Replimune that include visa sponsorship?
The most reliable approach is to search Migrate Mate, which aggregates verified sponsoring employers so you can confirm Replimune's sponsorship history before applying. Replimune's own careers page also lists current openings and typically notes visa sponsorship eligibility in the job description. Cross-referencing both sources gives you the clearest picture of available sponsored positions.
How do I approach the application timeline when targeting a sponsored role at Replimune?
Plan well ahead of any visa deadline. H-1B petitions are subject to an annual lottery with a filing window in early April for an October 1 start date, so aligning your job search to that calendar is critical. For TN or Green Card pathways, timelines differ but can still span several months. Engage early with Replimune's recruiting team about sponsorship intent and be transparent about your visa situation from the first conversation.
See which Replimune employers are hiring and sponsoring visas right now.
Search Replimune Jobs