Manufacturing Engineer Visa Sponsorship Jobs in Missouri
Missouri's manufacturing sector spans automotive supply chains in the Kansas City metro, aerospace components near St. Louis, and food processing operations statewide. Major employers including Boeing, General Motors, and Emerson Electric have sponsored manufacturing engineers through H-1B visa and other work visa programs, making Missouri a consistent destination for internationally trained engineers seeking sponsorship.
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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 Engineer Job Roles in Missouri
See all 124+ Manufacturing Engineer Jobs in Missouri
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Search Manufacturing Engineer Jobs in MissouriManufacturing Engineer Jobs in Missouri: Frequently Asked Questions
Which companies sponsor visas for manufacturing engineers in Missouri?
Boeing's St. Louis operations, Emerson Electric, General Motors, Anheuser-Busch InBev, and smaller Tier 1 and Tier 2 automotive suppliers in the Kansas City region have filed H-1B Labor Condition Applications for manufacturing engineer roles in Missouri. Aerospace and defense contractors operating near Lambert-St. Louis International Airport are particularly active sponsors for process and systems engineering positions.
Which visa types are most common for manufacturing engineer roles in Missouri?
The H-1B is the most common visa category for manufacturing engineers in Missouri, as the role typically qualifies as a specialty occupation requiring a bachelor's degree in mechanical, industrial, or manufacturing engineering. Candidates from Canada and Mexico may qualify for the TN visa under the engineer category. Australians may be eligible for the E-3 visa. All three require employer sponsorship before you can apply.
Which cities in Missouri have the most manufacturing engineer sponsorship jobs?
St. Louis and Kansas City account for the majority of manufacturing engineer sponsorship activity in Missouri. St. Louis draws heavily from aerospace and defense manufacturing, anchored by Boeing and a dense network of defense contractors. Kansas City has a strong automotive and food manufacturing presence. Columbia and Joplin also have manufacturing facilities, though sponsorship volume there is lower than in the two major metros.
How to find manufacturing engineer visa sponsorship jobs in Missouri?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can browse manufacturing engineer roles in Missouri without sifting through positions that don't offer sponsorship. Rather than applying broadly and asking about sponsorship later, Migrate Mate surfaces employers who have an active history of sponsoring international engineering candidates, which is especially useful in Missouri's aerospace and automotive manufacturing sectors.
Are there any Missouri-specific considerations for manufacturing engineers seeking visa sponsorship?
Missouri's manufacturing base is heavily concentrated in aerospace and automotive supply chains, which means many sponsoring employers are large primes or Tier 1 contractors with established immigration processes. Missouri universities, including Missouri University of Science and Technology and Washington University in St. Louis, produce engineering graduates who sometimes transition from OPT into sponsored positions with in-state manufacturers, creating a visible pipeline employers are already familiar with.
What is the prevailing wage for sponsored manufacturing engineer 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.