Product Consultant Visa Sponsorship Jobs in Oregon
Product consultant roles in Oregon are concentrated in Portland's tech corridor, where companies like Nike, Daimler Trucks North America, and a dense cluster of SaaS and cloud firms regularly hire for these positions. Intel's Hillsboro campus and Oregon Health & Science University also drive demand for product-facing consultants with specialized domain expertise.
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Get Access To All JobsTHE POSITION
Genentech’s Hillsboro Oregon campus—Hillsboro Innovative Therapies (HIT)—serves as a critical hub for emerging cell & gene therapy manufacturing. Housed within a modern 75-acre facility just outside Portland, HIT is at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities, aligning with Genentech’s mission to bring transformative therapies to patients.
As part of Genentech’s Cell and Gene Therapy community, this role offers the opportunity to shape and scale advanced therapy platforms through cross-site collaboration, data-driven innovation, and continuous improvement. This leader will play a pivotal role in defining and executing the MSAT strategy for cell therapy, guiding decisions, influencing global technology platforms, and representing HIT in strategic Roche network initiatives.
The Opportunity:
As the Head of Product Science and Lab Operations, you will lead a team of scientists and engineers within the Manufacturing Science and Technology (MSAT) function, focused on process science, technology transfer, and process validation strategy for cell therapy manufacturing. This team plays a pivotal role in enabling right-first-time manufacturing through data-driven process design, lifecycle validation, deviation investigation, and continuous improvement. In this role, you will serve as the strategic leader for each of these areas from development through commercial manufacturing and will also be responsible for the MSAT laboratory.
In addition to site responsibilities, you will serve as a network-level thought partner, representing HIT in enterprise planning forums, platform strategy discussions, and cross-functional governance bodies. You will be accountable for establishing scalable and future-ready MSAT capabilities that enable Genentech’s growing cell therapy portfolio across the development and commercial lifecycle. Key responsibilities include:
- Developing and Aligning Strategies: Creating integrated technical strategies for advanced therapies across clinical, process, manufacturing, and analytic needs, while aligning with Genentech’s cell therapy platforms and Roche network goals.
- Driving Innovation and Scalability: Identifying and implementing platform technologies, automation tools, and global synergies to reduce cycle times, optimize COGS, and improve scalability, traceability, and speed-to-patient processes.
- Overseeing Process Validation and Technology Transfer: Leading end-to-end process validation strategies, executing process implementation plans, and championing global standards for technology transfer and manufacturing excellence.
- MSAT Laboratory Leadership: Oversee and guide laboratory experiments and material characterization studies, ensuring scientific rigor, regulatory compliance, and alignment with clinical and commercial manufacturing needs. Provide technical direction to design and execute studies that generate critical process knowledge and support technology transfer.
- Allogeneic Donor Program Support: Provide technical leadership for allogeneic donor operations, including laboratory activities, donor material qualification, and process monitoring. Partner with clinical, supply chain, and manufacturing teams to ensure a reliable and compliant supply of qualified donors to meet program and production needs.
- Investigations and Troubleshooting: Lead complex process troubleshooting and deviation investigations using structured root cause analysis methodologies and advanced data analytics. Partner cross-functionally to identify, document, and implement corrective and preventive actions that drive robust, reliable, and compliant manufacturing operations.
- Collaborating Across Stakeholders: Partnering with QA, Regulatory, Manufacturing, and other teams to support lifecycle activities, regulatory filings, inspections, and global technical alignment.
- Mentoring and Developing Talent: Building, coaching, and engaging a high-performing team while fostering scientific rigor, leadership skills, GMP compliance, and innovation.
- Representing Genentech Globally: Acting as a technical leader in regulatory interactions, industry consortia, and governance boards to influence global regulatory and scientific advancements.
Who You Are:
- You possess a Bachelor’s degree in Cell Biology, Molecular Biology, Biochemical Engineering, or a related scientific discipline along with 12 years of direct relevant experience (or Master’s degree with 8+ years of directly relevant experience).
- You have at least 3 years of experience in cell therapy manufacturing, with 5+ years leading technical teams and managing cross-functional stakeholders.
- You possess a deep understanding of cell therapy platforms, process control, and regulatory expectations, including process validation, technology transfer, and lifecycle management.
- You have a proven track record of supporting regulatory submissions (e.g., IND, BLA) and health authority inspections.
- You possess expertise in advanced therapy medicinal products (ATMPs), including autologous and allogeneic workflows.
- You have experience with process monitoring and analytics tools (e.g., JMP, Spotfire, PI Historian) and MSAT lab operations (e.g., scale-down studies, closed-system modeling).
- You have experience leading data-driven scientific investigations and driving continuous improvement, digital integration, or innovation in regulated environments.
- You have demonstrated success influencing technical strategy across sites or global teams.
Relocation is approved for this posting.
This is an on-site position; no remote options are offered at this time.
The expected salary range for this position based on the primary location of Oregon is $151,600 - $281,500. 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 in this link.
LI-CA1
ptcareers
cellandgenetherapycareers
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 Facilities
Schedule Full time
Job Type Regular
Posted Date May 27th 2026
Job ID 202605-113449
THE POSITION
Genentech’s Hillsboro Oregon campus—Hillsboro Innovative Therapies (HIT)—serves as a critical hub for emerging cell & gene therapy manufacturing. Housed within a modern 75-acre facility just outside Portland, HIT is at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities, aligning with Genentech’s mission to bring transformative therapies to patients.
As part of Genentech’s Cell and Gene Therapy community, this role offers the opportunity to shape and scale advanced therapy platforms through cross-site collaboration, data-driven innovation, and continuous improvement. This leader will play a pivotal role in defining and executing the MSAT strategy for cell therapy, guiding decisions, influencing global technology platforms, and representing HIT in strategic Roche network initiatives.
The Opportunity:
As the Head of Product Science and Lab Operations, you will lead a team of scientists and engineers within the Manufacturing Science and Technology (MSAT) function, focused on process science, technology transfer, and process validation strategy for cell therapy manufacturing. This team plays a pivotal role in enabling right-first-time manufacturing through data-driven process design, lifecycle validation, deviation investigation, and continuous improvement. In this role, you will serve as the strategic leader for each of these areas from development through commercial manufacturing and will also be responsible for the MSAT laboratory.
In addition to site responsibilities, you will serve as a network-level thought partner, representing HIT in enterprise planning forums, platform strategy discussions, and cross-functional governance bodies. You will be accountable for establishing scalable and future-ready MSAT capabilities that enable Genentech’s growing cell therapy portfolio across the development and commercial lifecycle. Key responsibilities include:
- Developing and Aligning Strategies: Creating integrated technical strategies for advanced therapies across clinical, process, manufacturing, and analytic needs, while aligning with Genentech’s cell therapy platforms and Roche network goals.
- Driving Innovation and Scalability: Identifying and implementing platform technologies, automation tools, and global synergies to reduce cycle times, optimize COGS, and improve scalability, traceability, and speed-to-patient processes.
- Overseeing Process Validation and Technology Transfer: Leading end-to-end process validation strategies, executing process implementation plans, and championing global standards for technology transfer and manufacturing excellence.
- MSAT Laboratory Leadership: Oversee and guide laboratory experiments and material characterization studies, ensuring scientific rigor, regulatory compliance, and alignment with clinical and commercial manufacturing needs. Provide technical direction to design and execute studies that generate critical process knowledge and support technology transfer.
- Allogeneic Donor Program Support: Provide technical leadership for allogeneic donor operations, including laboratory activities, donor material qualification, and process monitoring. Partner with clinical, supply chain, and manufacturing teams to ensure a reliable and compliant supply of qualified donors to meet program and production needs.
- Investigations and Troubleshooting: Lead complex process troubleshooting and deviation investigations using structured root cause analysis methodologies and advanced data analytics. Partner cross-functionally to identify, document, and implement corrective and preventive actions that drive robust, reliable, and compliant manufacturing operations.
- Collaborating Across Stakeholders: Partnering with QA, Regulatory, Manufacturing, and other teams to support lifecycle activities, regulatory filings, inspections, and global technical alignment.
- Mentoring and Developing Talent: Building, coaching, and engaging a high-performing team while fostering scientific rigor, leadership skills, GMP compliance, and innovation.
- Representing Genentech Globally: Acting as a technical leader in regulatory interactions, industry consortia, and governance boards to influence global regulatory and scientific advancements.
Who You Are:
- You possess a Bachelor’s degree in Cell Biology, Molecular Biology, Biochemical Engineering, or a related scientific discipline along with 12 years of direct relevant experience (or Master’s degree with 8+ years of directly relevant experience).
- You have at least 3 years of experience in cell therapy manufacturing, with 5+ years leading technical teams and managing cross-functional stakeholders.
- You possess a deep understanding of cell therapy platforms, process control, and regulatory expectations, including process validation, technology transfer, and lifecycle management.
- You have a proven track record of supporting regulatory submissions (e.g., IND, BLA) and health authority inspections.
- You possess expertise in advanced therapy medicinal products (ATMPs), including autologous and allogeneic workflows.
- You have experience with process monitoring and analytics tools (e.g., JMP, Spotfire, PI Historian) and MSAT lab operations (e.g., scale-down studies, closed-system modeling).
- You have experience leading data-driven scientific investigations and driving continuous improvement, digital integration, or innovation in regulated environments.
- You have demonstrated success influencing technical strategy across sites or global teams.
Relocation is approved for this posting.
This is an on-site position; no remote options are offered at this time.
The expected salary range for this position based on the primary location of Oregon is $151,600 - $281,500. 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 in this link.
LI-CA1
ptcareers
cellandgenetherapycareers
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 Facilities
Schedule Full time
Job Type Regular
Posted Date May 27th 2026
Job ID 202605-113449
Product Consultant Job Roles in Oregon
See all Product Consultant Jobs in Oregon
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Search Product Consultant Jobs in OregonProduct Consultant Jobs in Oregon: Frequently Asked Questions
Which companies in Oregon sponsor visas for product consultants?
Nike, Intel, Daimler Trucks North America, and Portland-based SaaS companies such as Puppet and Jama Software have histories of H-1B visa sponsorship for product-oriented roles. Oregon Health & Science University sponsors product and implementation consultants in the healthcare technology space. Sponsorship willingness varies by company size, budget cycle, and whether the role meets specialty occupation standards, so researching each employer's prior filings is worth doing before applying.
What visa types are most common for product consultant roles in Oregon?
The H-1B is the most frequently used visa category for product consultant roles in Oregon, provided the position requires a bachelor's degree or higher in a specific field such as computer science, business, or engineering. TN visas apply to Canadian and Mexican nationals in qualifying professional categories. Candidates already holding L-1 visa status through a multinational employer may also transfer into a product consultant role domestically without entering the H-1B lottery.
Which Oregon cities have the most product consultant visa sponsorship jobs?
Portland accounts for the large majority of product consultant sponsorship activity in Oregon, driven by its concentration of technology, retail-tech, and professional services employers. Hillsboro, home to Intel's largest U.S. campus, is the second most active city for these roles. Beaverton sees demand through Nike and adjacent vendors. Salem and Eugene have smaller but growing markets, particularly in healthcare IT and university-affiliated software organizations.
How to find product consultant visa sponsorship jobs in Oregon?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can search product consultant roles in Oregon without sorting through positions that don't support international candidates. Because sponsorship is confirmed at the listing level, you avoid applying to roles where visa support is unclear. Focusing your search on Portland and Hillsboro on Migrate Mate will surface the highest volume of relevant openings for this role in Oregon.
Are there state-specific factors that affect product consultant sponsorship in Oregon?
Oregon does not impose state-level visa sponsorship requirements beyond federal obligations, but employers must comply with Department of Labor prevailing wage rules when filing a Labor Condition Application for H-1B roles. Portland's competitive tech hiring market means prevailing wages for product consultants are benchmarked against a metropolitan area with relatively high compensation norms. Oregon's pipeline of graduates from Portland State University, University of Oregon, and Oregon State University also keeps local employer demand for sponsored product talent active year-round.
What is the prevailing wage for sponsored product consultant jobs in Oregon?
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.