Manufacturing Technician Visa Sponsorship Jobs in Missouri
Missouri's manufacturing sector spans aerospace components in St. Louis, automotive parts in Kansas City, and industrial equipment across Springfield and Joplin. Major employers like Boeing, General Motors, and Emerson Electric have hired manufacturing technicians with visa sponsorship. The state's concentration of advanced manufacturing facilities creates consistent demand for skilled technicians from overseas.
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Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
Position Summary
We have an opportunity for a Commercial Manufacturing Quality Assurance Specialist to join our team. In this role, you will support quality operations by reviewing batch records, ensuring compliance with FDA guidelines, and maintaining high standards of product quality. You will contribute to continuous improvement initiatives and collaborate with cross-functional teams to uphold regulatory and internal standards. This position offers the chance to make a meaningful impact in a dynamic, science-driven environment.
Shift: M-F 6am-2pm
Location: Kansas City, MO
100% Onsite
The Role
- Perform batch record review, product release, and disposition.
- Draft, review, and approve technical documents such as procedures or master batch records.
- Ensure that products are manufactured, tested, and released according to applicable FDA guidelines, regulations, GXPs, and internal standard operating procedures.
- Participate in the development and maintenance of quality assurance programs, procedures, and controls to ensure that products meet established standards and agency guidelines.
- Train, coach, and mentor others on technical, personal development, or business issues.
- Assist in data compilation for annual product review.
- Provide quality assurance advisement for project outcomes and customer interactions.
- Participate in the development and implementation of process-related improvements.
- Assist with manufacturing floor activities, including equipment and room approval and facility compliance.
- Perform other duties as assigned.
The Candidate
Minimum Requirements
- Master’s degree in a scientific discipline with no experience, or Bachelor’s degree in a scientific discipline with 1+ years of experience in Quality Assurance, Quality Control, or Regulatory Compliance in a Good Manufacturing Practice environment, or Associate’s degree with 3+ years of experience in an FDA-regulated field and 1+ years in Quality Assurance, Quality Control, or Regulatory Compliance, or high school diploma with 5+ years of experience in an FDA-regulated field and 1+ years in Quality Assurance, Quality Control, or Regulatory Compliance.
- Six Sigma or American Society for Quality certification preferred.
- Perform batch record review, product release, and disposition.
- Draft, review, and approve technical documents such as procedures or master batch records.
- Participate in the development and maintenance of quality assurance programs, procedures, and controls to ensure that products meet established standards and agency guidelines.
- Provide quality assurance advisement for project outcomes and customer interactions.
- Participate in the development and implementation of process-related improvements.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
About Site
Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
Position Summary
We have an opportunity for a Commercial Manufacturing Quality Assurance Specialist to join our team. In this role, you will support quality operations by reviewing batch records, ensuring compliance with FDA guidelines, and maintaining high standards of product quality. You will contribute to continuous improvement initiatives and collaborate with cross-functional teams to uphold regulatory and internal standards. This position offers the chance to make a meaningful impact in a dynamic, science-driven environment.
Shift: M-F 6am-2pm
Location: Kansas City, MO
100% Onsite
The Role
- Perform batch record review, product release, and disposition.
- Draft, review, and approve technical documents such as procedures or master batch records.
- Ensure that products are manufactured, tested, and released according to applicable FDA guidelines, regulations, GXPs, and internal standard operating procedures.
- Participate in the development and maintenance of quality assurance programs, procedures, and controls to ensure that products meet established standards and agency guidelines.
- Train, coach, and mentor others on technical, personal development, or business issues.
- Assist in data compilation for annual product review.
- Provide quality assurance advisement for project outcomes and customer interactions.
- Participate in the development and implementation of process-related improvements.
- Assist with manufacturing floor activities, including equipment and room approval and facility compliance.
- Perform other duties as assigned.
The Candidate
Minimum Requirements
- Master’s degree in a scientific discipline with no experience, or Bachelor’s degree in a scientific discipline with 1+ years of experience in Quality Assurance, Quality Control, or Regulatory Compliance in a Good Manufacturing Practice environment, or Associate’s degree with 3+ years of experience in an FDA-regulated field and 1+ years in Quality Assurance, Quality Control, or Regulatory Compliance, or high school diploma with 5+ years of experience in an FDA-regulated field and 1+ years in Quality Assurance, Quality Control, or Regulatory Compliance.
- Six Sigma or American Society for Quality certification preferred.
- Perform batch record review, product release, and disposition.
- Draft, review, and approve technical documents such as procedures or master batch records.
- Participate in the development and maintenance of quality assurance programs, procedures, and controls to ensure that products meet established standards and agency guidelines.
- Provide quality assurance advisement for project outcomes and customer interactions.
- Participate in the development and implementation of process-related improvements.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Manufacturing Technician Job Roles in Missouri
See all 74+ Manufacturing Technician Jobs in Missouri
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Search Manufacturing Technician Jobs in MissouriManufacturing Technician Jobs in Missouri: Frequently Asked Questions
Which companies sponsor visas for manufacturing technicians in Missouri?
Boeing in St. Louis is among the most active sponsors for manufacturing technicians in Missouri, particularly for aerospace assembly and quality roles. General Motors and Ford have sponsored technicians at Kansas City area facilities. Emerson Electric, Anheuser-Busch InBev, and Leggett and Platt have also filed Labor Condition Applications for manufacturing technician positions in Missouri, according to Department of Labor disclosure data.
Which visa types are most common for manufacturing technician roles in Missouri?
The H-1B visa is the most common visa for manufacturing technicians in Missouri when the role requires a bachelor's degree in engineering, industrial technology, or a related field and qualifies as a specialty occupation. The TN visa is available to Canadian and Mexican nationals in qualifying engineering technician roles. The O-1 visa is rarely applicable for technician positions, and the EB-3 employment-based green card is a common immigrant pathway for skilled manufacturing workers.
Which cities in Missouri have the most manufacturing technician sponsorship jobs?
St. Louis leads Missouri for manufacturing technician sponsorship opportunities, driven by aerospace, defense, and chemicals industries concentrated there. Kansas City is the second-largest hub, with automotive manufacturing and food processing employers active in sponsorship. Springfield supports a smaller but growing base of industrial and consumer goods manufacturers. Joplin and Cape Girardeau also have manufacturing presence, though sponsorship activity there is more limited.
How to find manufacturing technician visa sponsorship jobs in Missouri?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can search manufacturing technician roles in Missouri without sorting through positions that don't sponsor. The platform aggregates openings from employers with documented sponsorship histories, which is particularly useful in Missouri where sponsoring manufacturers are spread across multiple metro areas. Filtering by role and state on Migrate Mate saves significant time compared to unfiltered searches.
Are there state-specific considerations for manufacturing technician visa sponsorship in Missouri?
Missouri's manufacturing economy is heavily tied to aerospace, automotive, and agribusiness, so technician roles often require specialized certifications relevant to those industries, such as FAA repair station credentials for aerospace work in St. Louis. Missouri does not have state-level immigration programs, so sponsorship depends entirely on individual employers. University of Missouri and Missouri University of Science and Technology produce engineering graduates who sometimes transition into technician roles, creating employer pipelines that occasionally extend to sponsored international candidates.
What is the prevailing wage for sponsored manufacturing technician jobs in Missouri?
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.