Manufacturing Process Engineer Jobs in USA with Visa Sponsorship
Manufacturing Process Engineers qualify for H-1B visa, E-3 visa, and TN visas through specialty occupation requirements. Most positions require an engineering degree in chemical, mechanical, or industrial engineering. Major manufacturers like Boeing, Ford, and 3M regularly sponsor visas for process optimization, quality control, and production efficiency roles. For detailed occupation requirements, see the O*NET profile.
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Get Access To All JobsFacility: Manufacturing
Location: Clayton, NC, US
About the Department
At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At PS AM, you’ll join a global network of manufacturing professionals who are passionate about what they do.
What we offer you:
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.
The Position
Operate manufacturing equipment in order to achieve production goals.
Relationships
Reports to Shift Manager.
Essential Functions
- Set up, operate, monitor & control equipment, systems & processes associated with production/manufacturing lines
- Execution of production schedule to achieve production goals
- Maintain production areas & perform cleaning
- Actively participate in & support event response
- Review & author SOP’s & other documents, as required
- Assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance
- Record/review production data in BPR’s and associated forms
- Follow all safety & environmental requirements in the performance of duties
- Other accountabilities, as assigned
Physical Requirements
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Routinely operates & inspects manufacturing equipment using hands. Strap & unstrap pallets using hands. Must be able to be on your feet for up to a 12-hour shift. May require corrected vision to 20/20 or 20/25 based on role. May require colour vision based on role. Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. May be required to wear latex gloves. May perform critical job functions in extremely cold work environments depending on site. May position oneself within confined spaces for inspection if required of the role. Ability to work in loud noise environments with hearing protection. May be required to secure a motorized vehicle license & operate a motorized vehicle based on the role.
Qualifications
- High school diploma or equivalent required
- Minimum of six (6) months manufacturing experience required
- Minimum experience requirement may be waived with military experience, a BioWorks/BioBlend certification/equivalent from an accredited college, or a current Novo Nordisk contractor that has 3 months of demonstrated performance in the relevant area
- Experience working in an FDA regulated environment preferred
- Production/Manufacturing experience preferred
- Ability to read, write & understand product documentation & standard operating procedures with attention to detail required
- Computer literacy preferred
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
Facility: Manufacturing
Location: Clayton, NC, US
About the Department
At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At PS AM, you’ll join a global network of manufacturing professionals who are passionate about what they do.
What we offer you:
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.
The Position
Operate manufacturing equipment in order to achieve production goals.
Relationships
Reports to Shift Manager.
Essential Functions
- Set up, operate, monitor & control equipment, systems & processes associated with production/manufacturing lines
- Execution of production schedule to achieve production goals
- Maintain production areas & perform cleaning
- Actively participate in & support event response
- Review & author SOP’s & other documents, as required
- Assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance
- Record/review production data in BPR’s and associated forms
- Follow all safety & environmental requirements in the performance of duties
- Other accountabilities, as assigned
Physical Requirements
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Routinely operates & inspects manufacturing equipment using hands. Strap & unstrap pallets using hands. Must be able to be on your feet for up to a 12-hour shift. May require corrected vision to 20/20 or 20/25 based on role. May require colour vision based on role. Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. May be required to wear latex gloves. May perform critical job functions in extremely cold work environments depending on site. May position oneself within confined spaces for inspection if required of the role. Ability to work in loud noise environments with hearing protection. May be required to secure a motorized vehicle license & operate a motorized vehicle based on the role.
Qualifications
- High school diploma or equivalent required
- Minimum of six (6) months manufacturing experience required
- Minimum experience requirement may be waived with military experience, a BioWorks/BioBlend certification/equivalent from an accredited college, or a current Novo Nordisk contractor that has 3 months of demonstrated performance in the relevant area
- Experience working in an FDA regulated environment preferred
- Production/Manufacturing experience preferred
- Ability to read, write & understand product documentation & standard operating procedures with attention to detail required
- Computer literacy preferred
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
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Get Access To All JobsTips for Finding Visa Sponsorship as a Manufacturing Process Engineer
Target specialty occupation alignment
Emphasize process optimization, statistical analysis, and technical problem-solving in your applications. These specialized skills clearly differentiate manufacturing engineering from general production roles that may not qualify for visa sponsorship.
Highlight Six Sigma and lean manufacturing certifications
Advanced certifications demonstrate specialized knowledge beyond basic manufacturing. Green Belt, Black Belt, or lean manufacturing credentials strengthen your specialty occupation case and appeal to efficiency-focused employers.
Focus on companies with complex manufacturing processes
Aerospace, automotive, pharmaceuticals, and semiconductor companies have intricate processes requiring specialized engineering expertise. These industries regularly sponsor visas compared to simpler manufacturing operations.
Demonstrate measurable process improvements
Quantify your impact through cycle time reduction, yield improvements, or cost savings. Concrete metrics prove your specialized value to hiring managers and strengthen the business necessity for sponsorship.
Consider manufacturing hubs with established sponsorship patterns
States like Michigan, Ohio, Texas, and California have dense manufacturing sectors with visa sponsorship experience. Established manufacturing regions often have streamlined immigration processes through local law firms.
Understand degree equivalency for international engineering programs
Three-year international engineering degrees may need credential evaluation for U.S. visa applications. Research WES, ECE, or other evaluation services early to avoid delays in your sponsorship timeline.
Frequently Asked Questions
What engineering degree do I need for Manufacturing Process Engineer visa sponsorship?
Most positions require a bachelor's degree in chemical, mechanical, industrial, or manufacturing engineering. Some employers accept related fields like materials science or operations research. The degree must directly relate to process engineering responsibilities like statistical analysis, quality control, and production optimization to satisfy specialty occupation requirements.
Do Manufacturing Process Engineers get approved for H-1B visas?
Yes, Manufacturing Process Engineers typically qualify as specialty occupations when the role involves complex technical analysis, process optimization, and engineering problem-solving. Approval rates are strong for positions requiring specialized knowledge of manufacturing systems, quality control methodologies, or advanced process improvement techniques rather than routine production oversight.
Can I get TN visa sponsorship as a Manufacturing Process Engineer?
Canadian and Mexican citizens can qualify under the TN "Engineer" category with an engineering degree and job duties focused on process design, optimization, or technical analysis. The position must require engineering expertise rather than general manufacturing management. Most process engineering roles at established manufacturers meet these requirements.
How to find Manufacturing Process Engineer jobs with visa sponsorship?
To find Manufacturing Process Engineer positions with visa sponsorship, use Migrate Mate, which specializes in connecting international candidates with sponsoring employers. Focus your search on automotive, pharmaceutical, semiconductor, and aerospace companies, as they frequently sponsor H-1B visa and other work visas for process engineers. Large manufacturing corporations and multinational companies often have established visa sponsorship programs for technical roles.
Which companies sponsor Manufacturing Process Engineers for work visas?
Major manufacturers like Boeing, Ford, General Motors, 3M, Intel, and pharmaceutical companies regularly sponsor process engineers. Automotive, aerospace, semiconductor, and chemical industries have the highest sponsorship rates due to complex manufacturing processes requiring specialized engineering expertise. Defense contractors also sponsor frequently but may require security clearance eligibility.
What if my manufacturing experience is in a different engineering discipline?
Cross-disciplinary experience can strengthen your application if you can demonstrate how your background applies to process engineering. For example, mechanical engineers transitioning to manufacturing process roles should emphasize thermodynamics, fluid mechanics, or automation experience. The key is showing specialized knowledge transfer rather than general manufacturing oversight.
What is the prevailing wage requirement for sponsored Manufacturing Process Engineer jobs?
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.