eGenesis Visa Sponsorship Jobs USA
eGenesis is a biotechnology company pioneering xenotransplantation research, working to make human-compatible organs from genetically engineered animals. For visa-sponsored scientists and researchers, eGenesis has sponsored H-1B visas and welcomes candidates on F-1 OPT, F-1 CPT, and TN visa status.
Find eGenesis JobsOverview
Showing 4 of 5+ eGenesis Visa Sponsorship Jobs USA
See all eGenesis Visa Sponsorship Jobs USA
Sign up for free to unlock all listings, filter by visa type, and get alerts for new eGenesis Visa Sponsorship Jobs USA.
Get Access To All JobsAbout EGenesis
eGenesis is a clinical-stage biotechnology company developing human-compatible engineered organs to address the severe global organ shortage. The Company’s proprietary genome engineering platform enables extensive, multiplex gene edits to remove key biological barriers, add protective human transgenes, and inactivate endogenous retroviruses. EGEN-2784, a genetically engineered porcine kidney, is the Company’s lead program and is currently being evaluated in a multi-patient Expanded Access study at MGH. eGenesis is headquartered in Cambridge, MA. At eGenesis, our core values—innovation, collaboration, compassion, resilience, and passion—are at the center of how we work. We engineer hope and bring passion to everything we do. We collaborate and learn from one another, combining diverse expertise to tackle complex challenges. We innovate boldly, pushing boundaries and science to new heights. where no pig organ has gone before. With resilience, we navigate challenges and celebrate progress together. And in all we do, we lead with compassion—for our patients, our people, and our pigs.
Position Summary
The Senior Quality Systems Specialist will be supporting the QA team to implement and manage Quality Systems supporting GMP Manufacturing and Testing across all eGenesis locations. This position reports to the Associate Director of Quality Systems and is a highly visible and impactful position that will require cross-functional interaction across the multiple teams in the Organization. This position will be in Cambridge, MA.
Responsibilities
- Developing, implementing, and maintaining processes to support QA oversight for the manufacturing of material to be used in clinical studies
- Ability to initiate, support and manage deviations and CAPAs ensuring timely closure across all sites
- Management and Administration of the Electronic Laboratory Notebook used for issuance and execution of Batch Records and Test Methods
- Responsible for Documentation Management (archival of physical records, management of Document Change Controls etc.)
- Responsible for Organization Training including administering training, managing training matrices, trending metrics and further developing the Training Program
- Participating in cross-functional teams to resolve quality related issues impacting manufacturing activities
- Developing, trending, and reporting of relevant Quality Metrics associated with the area of responsibility
- Supporting the development of policies, processes, procedures, and controls ensuring they conform to established cGMP standards and regulatory requirements and guidelines
- Provide Quality Assurance support to many cross functional teams including Development, Manufacturing, Quality Control departments
- Provide mentoring and training to staff that are new to regulatory requirements and to facilitate their use of established quality systems
- Implement process improvements to enhance compliance and improve method and product quality processes (e.g. process tools creation, SOP revision, or enterprise systems implementation)
- Provide Quality Assurance support in reviewing/approving executed records in needed areas (Forms, Logbooks, Master Batch Records etc.)
- Perform duties regarding special projects, as assigned by QA Management
Technical Qualifications
- Bachelor’s degree in a scientific or operational discipline relevant to the life sciences or biopharma areas with 5+ years combined of experience in quality system management
- Non-degreed candidates with 7+ years combined of relevant GLP/GMP quality systems experience will be considered
- Knowledge of Quality Management Systems (QMS), CAPA processes, and audit procedures
- Familiarity with relevant regulations and standards (e.g., ISO, FDA, cGMP)
- Strong analytical, problem-solving, and communication skills
- Proficiency in using QA software tools and electronic Quality Management Systems (eQMS) is a plus
Preferred Qualifications
- Experience in Qualio, Veeva and/or Benchling
- Experience in a start-up or small company environment
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About EGenesis
eGenesis is a clinical-stage biotechnology company developing human-compatible engineered organs to address the severe global organ shortage. The Company’s proprietary genome engineering platform enables extensive, multiplex gene edits to remove key biological barriers, add protective human transgenes, and inactivate endogenous retroviruses. EGEN-2784, a genetically engineered porcine kidney, is the Company’s lead program and is currently being evaluated in a multi-patient Expanded Access study at MGH. eGenesis is headquartered in Cambridge, MA. At eGenesis, our core values—innovation, collaboration, compassion, resilience, and passion—are at the center of how we work. We engineer hope and bring passion to everything we do. We collaborate and learn from one another, combining diverse expertise to tackle complex challenges. We innovate boldly, pushing boundaries and science to new heights. where no pig organ has gone before. With resilience, we navigate challenges and celebrate progress together. And in all we do, we lead with compassion—for our patients, our people, and our pigs.
Position Summary
The Senior Quality Systems Specialist will be supporting the QA team to implement and manage Quality Systems supporting GMP Manufacturing and Testing across all eGenesis locations. This position reports to the Associate Director of Quality Systems and is a highly visible and impactful position that will require cross-functional interaction across the multiple teams in the Organization. This position will be in Cambridge, MA.
Responsibilities
- Developing, implementing, and maintaining processes to support QA oversight for the manufacturing of material to be used in clinical studies
- Ability to initiate, support and manage deviations and CAPAs ensuring timely closure across all sites
- Management and Administration of the Electronic Laboratory Notebook used for issuance and execution of Batch Records and Test Methods
- Responsible for Documentation Management (archival of physical records, management of Document Change Controls etc.)
- Responsible for Organization Training including administering training, managing training matrices, trending metrics and further developing the Training Program
- Participating in cross-functional teams to resolve quality related issues impacting manufacturing activities
- Developing, trending, and reporting of relevant Quality Metrics associated with the area of responsibility
- Supporting the development of policies, processes, procedures, and controls ensuring they conform to established cGMP standards and regulatory requirements and guidelines
- Provide Quality Assurance support to many cross functional teams including Development, Manufacturing, Quality Control departments
- Provide mentoring and training to staff that are new to regulatory requirements and to facilitate their use of established quality systems
- Implement process improvements to enhance compliance and improve method and product quality processes (e.g. process tools creation, SOP revision, or enterprise systems implementation)
- Provide Quality Assurance support in reviewing/approving executed records in needed areas (Forms, Logbooks, Master Batch Records etc.)
- Perform duties regarding special projects, as assigned by QA Management
Technical Qualifications
- Bachelor’s degree in a scientific or operational discipline relevant to the life sciences or biopharma areas with 5+ years combined of experience in quality system management
- Non-degreed candidates with 7+ years combined of relevant GLP/GMP quality systems experience will be considered
- Knowledge of Quality Management Systems (QMS), CAPA processes, and audit procedures
- Familiarity with relevant regulations and standards (e.g., ISO, FDA, cGMP)
- Strong analytical, problem-solving, and communication skills
- Proficiency in using QA software tools and electronic Quality Management Systems (eQMS) is a plus
Preferred Qualifications
- Experience in Qualio, Veeva and/or Benchling
- Experience in a start-up or small company environment
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Job Roles at eGenesis
See all eGenesis Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new eGenesis roles.
Get Access To All JobsTips for Finding eGenesis Visa Sponsorship Jobs USA
Target roles that match eGenesis's core research focus
eGenesis works at the intersection of genomics, gene editing, and transplant biology. Scientists and researchers with backgrounds in CRISPR, molecular biology, or immunology align closely with the roles most likely to receive H-1B sponsorship consideration at the company.
Leverage your F-1 OPT or CPT window strategically
eGenesis sponsors F-1 OPT and CPT, making it accessible for international students early in their U.S. career. Starting on OPT gives you time to demonstrate value before the company pursues H-1B sponsorship on your behalf.
Canadian and Mexican candidates have a direct path via TN
eGenesis sponsors TN visas, which don't require a lottery and can often be obtained faster than H-1B. If you're a Canadian or Mexican scientist in a qualifying TN occupation, this can be the most practical entry point.
Highlight specialized technical skills in your application
At a company doing cutting-edge xenotransplantation research, generalist science backgrounds are less competitive. Emphasize domain-specific skills, published research, or lab experience directly relevant to organ engineering, gene editing, or transplant immunology.
Understand that sponsorship reflects genuine hiring need
eGenesis's sponsorship activity reflects focused, specialty hiring rather than high-volume recruiting. Each sponsored role tends to be highly specific, so tailoring your application to the exact research area in the job description significantly improves your chances.
Use Migrate Mate to find and track eGenesis openings
eGenesis doesn't always advertise widely for sponsored roles. Migrate Mate surfaces verified sponsors filtered by visa type and industry, so you can monitor eGenesis openings and apply as soon as a sponsored position in your research area becomes available.
Frequently Asked Questions
Does eGenesis sponsor H-1B visas?
Yes, eGenesis sponsors H-1B visas. The company operates in the Science & Research sector, specifically in xenotransplantation and gene editing, where specialized expertise is often sourced globally. H-1B sponsorship at eGenesis tends to be reserved for roles requiring highly specific scientific qualifications that align with their organ engineering research pipeline.
Which visa types does eGenesis sponsor?
eGenesis sponsors H-1B, F-1 OPT, F-1 CPT, and TN visas. This range covers international students completing degrees in the U.S., early-career researchers on OPT or CPT, Canadian and Mexican professionals eligible for TN status, and experienced scientists requiring H-1B sponsorship. Green Card sponsorship has not been a recent pattern for the company.
Which departments or roles at eGenesis are most likely to receive visa sponsorship?
Sponsorship at eGenesis is concentrated in scientific and research roles. Positions in molecular biology, genomics, immunology, animal science, and translational research are the most likely to be sponsored given the company's focus on developing genetically engineered pig organs for human transplantation. Technical laboratory and research associate positions are also plausible candidates.
How do I apply to eGenesis if I need visa sponsorship?
Start by identifying open roles that match your scientific background on Migrate Mate, which filters employers by verified sponsorship history so you're not wasting time on companies that don't sponsor. When applying to eGenesis, make your visa status clear upfront and emphasize research skills directly relevant to their xenotransplantation work. eGenesis is a focused, specialist employer, so a highly targeted application carries significantly more weight than a general one.
How do I know if eGenesis is actively hiring sponsored roles right now?
eGenesis hiring activity can be sporadic given the company's size and research stage. The best approach is to monitor their open positions consistently rather than applying in a single window. Migrate Mate tracks sponsoring employers and surfaces verified open roles, making it straightforward to stay current on eGenesis postings without manually checking multiple sources.