Genentech Visa Sponsorship USA
Genentech is one of the most established names in biotechnology and medical research, with a strong track record of sponsoring international talent across research, engineering, and clinical roles. For visa holders seeking a science-driven employer with real sponsorship commitment, Genentech is a standout option.
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Get Access To All JobsTHE POSITION
You, as a Cell and Gene Therapy Specialist I, are part of the Genentech San Diego internal manufacturing team in support of Genentech San Diego’s pre-clinical and clinical production of cell therapies. You will support process tech transfers, routine GMP production activities, and technology improvements towards the successful delivery of released product to meet the needs of Genentech San Diego’s clinical trials.
THE OPPORTUNITY
Work is generally performed in a GMP manufacturing facility. You are in a position that requires a combination of standing or sitting in a cleanroom manufacturing environment, as well as walking around the facility. You will work in controlled environments requiring special gowning. You are required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body.
In this role, you are:
- Performing critical GMP aseptic operations in Grade A and Grade B production environments by following batch records, SOPs, policies, and work instructions to ensure safety and compliance.
- Assisting in all areas of cell therapy operations, including stocking, tracking inventory, material movement, maintaining metrics, filling log sheets, and supporting special projects as needed.
- Supporting startup activities for a new cGMP facility by collaborating with Process Development, MSAT, Facilities, and Quality departments.
- Escalating processing and equipment issues when necessary, participating in deviation writing, root cause investigations, and implementing CAPAs when required.
- Collaborating with Supply Chain, Process Development, Facilities, and Quality teams to execute GMP operations while prioritizing a right-the-first-time philosophy and fostering a safety-first culture.
- Adhering to all SOPs, Work Instructions, and cGMP regulations, accurately documenting clinical manufacturing activities, and routinely cleaning cleanrooms, manufacturing support areas, and equipment.
- Operating and maintaining bench-top equipment, including tubing welders, tube sealers, cell counters, centrifuges, and other cell therapy process systems.
- Managing material processes and data entry for manufacturing metrics, participating in material management and bill of material activities, leading small manufacturing projects, and acting as a subject matter expert for minor equipment.
WHO YOU ARE
- Bachelor’s degree in biology, Chemistry, or Engineering preferred OR 2+ years of related GMP experience (an equivalent combination of education and experience may be considered)
- Experience in the biotechnology industry in a GMP environment is preferred. Prior experience with cell or gene therapy manufacturing is a plus
- Demonstrated aseptic techniques
- Able to lift 40 pounds and stand for hours at a time. Flexible to work off-shift hours, weekends, and some holiday work
BEHAVIORS, COMPETENCIES, AND QUALITIES OF THE IDEAL APPLICANT
- Demonstrating excellent proficiency in Microsoft Word, Excel, and PowerPoint to support various tasks and projects.
- Showing self-motivation and a positive attitude, with a willingness to take on temporary responsibilities outside the initial job description.
- Adapting to a fast-paced, constantly evolving environment while thinking creatively and proposing innovative solutions.
- Following verbal and written instructions accurately, ensuring effective communication and task execution.
- Applying strong problem-solving skills to address challenges and develop practical solutions.
- Collaborating effectively as a team player to contribute to collective goals and maintain a supportive work environment.
Relocation Benefits are not offered for this job posting.
The expected salary range for this position based on California is 43,300.00 - 80,300.00 USD Annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
JOB FACTS
Job Sub Category: Manufacturing
Schedule: Full time
Job Type: Regular
Posted Date: Mar 20th 2026
Job ID: 202603-106164
THE POSITION
You, as a Cell and Gene Therapy Specialist I, are part of the Genentech San Diego internal manufacturing team in support of Genentech San Diego’s pre-clinical and clinical production of cell therapies. You will support process tech transfers, routine GMP production activities, and technology improvements towards the successful delivery of released product to meet the needs of Genentech San Diego’s clinical trials.
THE OPPORTUNITY
Work is generally performed in a GMP manufacturing facility. You are in a position that requires a combination of standing or sitting in a cleanroom manufacturing environment, as well as walking around the facility. You will work in controlled environments requiring special gowning. You are required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body.
In this role, you are:
- Performing critical GMP aseptic operations in Grade A and Grade B production environments by following batch records, SOPs, policies, and work instructions to ensure safety and compliance.
- Assisting in all areas of cell therapy operations, including stocking, tracking inventory, material movement, maintaining metrics, filling log sheets, and supporting special projects as needed.
- Supporting startup activities for a new cGMP facility by collaborating with Process Development, MSAT, Facilities, and Quality departments.
- Escalating processing and equipment issues when necessary, participating in deviation writing, root cause investigations, and implementing CAPAs when required.
- Collaborating with Supply Chain, Process Development, Facilities, and Quality teams to execute GMP operations while prioritizing a right-the-first-time philosophy and fostering a safety-first culture.
- Adhering to all SOPs, Work Instructions, and cGMP regulations, accurately documenting clinical manufacturing activities, and routinely cleaning cleanrooms, manufacturing support areas, and equipment.
- Operating and maintaining bench-top equipment, including tubing welders, tube sealers, cell counters, centrifuges, and other cell therapy process systems.
- Managing material processes and data entry for manufacturing metrics, participating in material management and bill of material activities, leading small manufacturing projects, and acting as a subject matter expert for minor equipment.
WHO YOU ARE
- Bachelor’s degree in biology, Chemistry, or Engineering preferred OR 2+ years of related GMP experience (an equivalent combination of education and experience may be considered)
- Experience in the biotechnology industry in a GMP environment is preferred. Prior experience with cell or gene therapy manufacturing is a plus
- Demonstrated aseptic techniques
- Able to lift 40 pounds and stand for hours at a time. Flexible to work off-shift hours, weekends, and some holiday work
BEHAVIORS, COMPETENCIES, AND QUALITIES OF THE IDEAL APPLICANT
- Demonstrating excellent proficiency in Microsoft Word, Excel, and PowerPoint to support various tasks and projects.
- Showing self-motivation and a positive attitude, with a willingness to take on temporary responsibilities outside the initial job description.
- Adapting to a fast-paced, constantly evolving environment while thinking creatively and proposing innovative solutions.
- Following verbal and written instructions accurately, ensuring effective communication and task execution.
- Applying strong problem-solving skills to address challenges and develop practical solutions.
- Collaborating effectively as a team player to contribute to collective goals and maintain a supportive work environment.
Relocation Benefits are not offered for this job posting.
The expected salary range for this position based on California is 43,300.00 - 80,300.00 USD Annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
JOB FACTS
Job Sub Category: Manufacturing
Schedule: Full time
Job Type: Regular
Posted Date: Mar 20th 2026
Job ID: 202603-106164
Job Roles at Genentech Companies
How to Get Visa Sponsorship in Genentech Visa Sponsorship USA
Target roles that align with Genentech's core research functions
Genentech's sponsorship activity is concentrated in scientific, clinical, and technical roles. Focus your applications on positions in drug development, bioinformatics, regulatory affairs, and biomedical engineering, these departments have the strongest history of supporting international candidates.
Prepare for a structured, multi-stage interview process
Genentech's hiring pipeline for technical and research roles typically involves multiple rounds, including competency-based and scientific assessments. Start preparing early, the timeline from application to offer can extend several months, which matters if your OPT or status has a deadline.
Highlight your specialization in a therapeutic or research area
Genentech invests heavily in oncology, immunology, and neuroscience. Candidates who can demonstrate focused expertise in one of these areas, not just general lab skills, are better positioned to move through hiring and secure sponsorship consideration for specialized roles.
Use verified sponsorship data when searching for open roles
Not every job posting signals whether a company will sponsor. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, helping you focus your search on Genentech roles where international candidates have a genuine path forward.
Connect with Genentech's university and internship pipeline early
Genentech actively recruits through academic partnerships and internship programs that support CPT and OPT. If you're still in graduate school, pursuing a Genentech internship is a practical way to build a relationship before entering the full-time sponsorship process.
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Get Access To All JobsFrequently Asked Questions
Does Genentech sponsor H-1B visas?
Yes, Genentech sponsors H-1B visas and is one of the more active sponsors in the biotech and medical research sector. Sponsorship is most common in scientific, engineering, and clinical roles. If you're on F-1 OPT, Genentech has a track record of supporting the transition to H-1B status, though you should confirm sponsorship eligibility with the recruiter during early conversations.
Which visa types does Genentech sponsor?
Genentech sponsors H-1B visas, TN visas for Canadian and Mexican nationals, F-1 OPT and CPT for students, and immigrant visa pathways including EB-2 and EB-3 Green Cards. The mix of nonimmigrant and immigrant sponsorship makes Genentech a strong long-term option for international candidates who want both near-term work authorization and a path to permanent residence.
Which departments or roles at Genentech are most likely to receive visa sponsorship?
Sponsorship at Genentech is most prevalent in research and development, bioinformatics, regulatory affairs, clinical operations, and biomedical or process engineering. These are the functions where specialized technical skills are hardest to source domestically, making employers more willing to invest in sponsorship. General business or administrative roles are less frequently sponsored.
How do I find open roles at Genentech that offer visa sponsorship?
The most reliable approach is to search specifically for roles where sponsorship has been confirmed by actual filing history, not just what a job posting claims. Migrate Mate lets you browse Genentech's open positions filtered by verified sponsorship activity, so you're not guessing whether the company will support your visa. Pair that with a direct conversation with Genentech's recruiting team about your visa status early in the process.
What should I know about Genentech's sponsorship process before applying?
Genentech works with immigration counsel internally, which means the sponsorship process is relatively structured once you have an offer. The key is timing, if you're on OPT, factor in when your authorization expires relative to the H-1B cap registration window in March. For Green Card sponsorship, EB-2 is more common for research-track roles, while EB-3 is used for some technical positions. Clarify the pathway with your hiring manager after receiving an offer.
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