Manufacturing Supervisor Visa Sponsorship Jobs in Texas
Texas is one of the most active states for manufacturing supervisor visa sponsorship, with major employers in the petrochemical corridor along the Gulf Coast, automotive and electronics manufacturing in the Dallas-Fort Worth metroplex, and semiconductor facilities in Austin and San Antonio. Companies like Samsung, Toyota, and LyondellBasell regularly hire internationally for supervisory production roles.
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Get Access To All JobsManufacturing Supervisor - Cell Therapy
Location: Houston, Texas – Onsite
Shift: 7 am - 7 pm – 12-hour rotating schedule.
As a Manufacturing Supervisor in Cell Therapy, you will lead frontline production teams and play a critical role in delivering high-quality, life-saving therapies under cGMP conditions. This role offers the opportunity to combine people leadership, technical expertise, and cross-functional collaboration in a fast-paced, highly regulated manufacturing environment.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:
- Performance-related bonus
- Medical, dental and vision insurance
- 401(k) matching plan
- Life insurance, as well as short-term and long-term disability insurance
- Employee assistance programs
- Paid time off (PTO)
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
What you will do:
- Lead and direct daily cell therapy manufacturing operations, ensuring safety, quality, and delivery to plan under cGMP conditions.
- Plan, schedule, and assign work for operators while providing real-time support, troubleshooting, and decision-making on the production floor.
- Coordinate activities across Manufacturing, Quality, Engineering, and other support teams to ensure on-time batch release and issue resolution.
- Own inspection readiness and compliance, including review and approval of batch records, logbooks, and SOPs to support right-first-time execution.
- Coach, train, and develop a team of 6–12 direct reports (and up to 20 dotted-line reports), including performance management and career development.
- Demonstrate technical leadership in cGMP compliance, deviation initiation and closure, and continuous improvement initiatives such as 6S and Lean.
- Act as shift leadership coverage as needed, supporting run manager responsibilities during absences or vacations.
What we are looking for:
- Bachelor’s degree is required.
- Proven experience leading manufacturing operations in a regulated environment, preferably cGMP or biopharmaceutical production.
- Strong people leadership skills, with the ability to coach, develop, and motivate teams in a shift-based operation.
- Solid understanding of production process flow, batch documentation, and quality systems in a highly regulated setting.
- Demonstrated ability to make sound decisions, troubleshoot non-routine issues, and collaborate cross-functionally.
- Effective written and verbal communication skills, including technical writing (e.g., deviations, SOPs).
- A continuous improvement mindset, with experience or interest in Lean, 6S, or Six Sigma methodologies preferred.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Manufacturing Supervisor - Cell Therapy
Location: Houston, Texas – Onsite
Shift: 7 am - 7 pm – 12-hour rotating schedule.
As a Manufacturing Supervisor in Cell Therapy, you will lead frontline production teams and play a critical role in delivering high-quality, life-saving therapies under cGMP conditions. This role offers the opportunity to combine people leadership, technical expertise, and cross-functional collaboration in a fast-paced, highly regulated manufacturing environment.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer:
- Performance-related bonus
- Medical, dental and vision insurance
- 401(k) matching plan
- Life insurance, as well as short-term and long-term disability insurance
- Employee assistance programs
- Paid time off (PTO)
Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
What you will do:
- Lead and direct daily cell therapy manufacturing operations, ensuring safety, quality, and delivery to plan under cGMP conditions.
- Plan, schedule, and assign work for operators while providing real-time support, troubleshooting, and decision-making on the production floor.
- Coordinate activities across Manufacturing, Quality, Engineering, and other support teams to ensure on-time batch release and issue resolution.
- Own inspection readiness and compliance, including review and approval of batch records, logbooks, and SOPs to support right-first-time execution.
- Coach, train, and develop a team of 6–12 direct reports (and up to 20 dotted-line reports), including performance management and career development.
- Demonstrate technical leadership in cGMP compliance, deviation initiation and closure, and continuous improvement initiatives such as 6S and Lean.
- Act as shift leadership coverage as needed, supporting run manager responsibilities during absences or vacations.
What we are looking for:
- Bachelor’s degree is required.
- Proven experience leading manufacturing operations in a regulated environment, preferably cGMP or biopharmaceutical production.
- Strong people leadership skills, with the ability to coach, develop, and motivate teams in a shift-based operation.
- Solid understanding of production process flow, batch documentation, and quality systems in a highly regulated setting.
- Demonstrated ability to make sound decisions, troubleshoot non-routine issues, and collaborate cross-functionally.
- Effective written and verbal communication skills, including technical writing (e.g., deviations, SOPs).
- A continuous improvement mindset, with experience or interest in Lean, 6S, or Six Sigma methodologies preferred.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Manufacturing Supervisor Job Roles in Texas
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Search Manufacturing Supervisor Jobs in TexasManufacturing Supervisor Jobs in Texas: Frequently Asked Questions
Which companies sponsor visas for manufacturing supervisors in Texas?
Texas-based manufacturers with documented H-1B visa and employment-based sponsorship activity include Samsung Austin Semiconductor, Toyota Motor Manufacturing Texas in San Antonio, LyondellBasell and BASF along the Houston petrochemical corridor, and Texas Instruments in Dallas. Large multinational manufacturers operating multiple facilities tend to have established immigration infrastructure and sponsor supervisory roles more consistently than smaller regional plants.
Which visa types are most common for manufacturing supervisor roles in Texas?
The H-1B is the most common visa category for manufacturing supervisors, provided the role requires at least a bachelor's degree in engineering, industrial management, or a related technical field. Supervisory roles that are primarily operational without a degree requirement may not qualify as a specialty occupation. The EB-3 employment-based green card is also used for skilled manufacturing positions where the employer is willing to sponsor permanent residence.
Which cities in Texas have the most manufacturing supervisor sponsorship jobs?
Houston leads the state due to its concentration of petrochemical, energy, and industrial manufacturing operations. Dallas-Fort Worth follows closely, with electronics, aerospace, and automotive suppliers driving demand for supervisory talent. San Antonio has grown significantly with Toyota's assembly plant and a broader automotive supply chain. Austin is emerging as a hub for semiconductor and advanced electronics manufacturing, particularly with Samsung's ongoing expansion.
How to find manufacturing supervisor visa sponsorship jobs in Texas?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it straightforward to find manufacturing supervisor roles in Texas without sorting through positions that don't sponsor. You can narrow results by location within Texas and by role type. Because sponsorship eligibility depends heavily on how the employer classifies the position, focusing on companies with prior H-1B or EB-3 filing history in manufacturing is a practical starting point.
Are there any Texas-specific considerations for manufacturing supervisor visa sponsorship?
Texas has no state income tax, which affects how employers calculate total compensation packages relative to prevailing wage requirements under the H-1B Labor Condition Application. The state's right-to-work status and large manufacturing base mean supervisory roles span diverse industries, but roles in petrochemicals and semiconductors tend to have the clearest degree requirements that support H-1B specialty occupation classification. Proximity to the Mexico border also means some facilities operate under specific trade compliance frameworks that can affect hiring timelines.
What is the prevailing wage for sponsored manufacturing supervisor jobs in Texas?
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.