Manufacturing Jobs at Catalent Pharma Solutions with Visa Sponsorship
Manufacturing roles at Catalent Pharma Solutions span production, quality operations, and process engineering across a global network of pharmaceutical and biologics facilities. Catalent has a consistent track record of sponsoring work visas for qualified manufacturing professionals, making it a strong target for international candidates building careers in pharma sciences.
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Get Access To All JobsSenior Manufacturing Product Lead
Position Summary
- Work Schedule: first shift, Monday to Friday
- 100% on-site in Kansas City
Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics.
The Role
- Collaborates cross-functionally with Manufacturing, Engineering, Maintenance, EHS and Quality to optimize productivity, safety, product quality and supply reliability for commercial products in compliance with cGMPs.
- Ensures commercial drug product manufacturing is Ready to Execute (RTE): Authors, reviews and approves commercial product manufacturing master batch records, BOMs, equipment recipes and cleaning verification forms as necessary to ensure RTE reliability.
- Partner with commercial clients as required on technical issues affecting their drug product(s). Act as product technical steward on client interactions.
- Provides technical support for process manufacturing areas, including investigation and correction of product/process-related problems and deviations, process troubleshooting and improvements.
- Serves as a subject matter expert during internal audits and regulatory inspections for technical aspects of the drug product process.
- Responsible for identifying, executing and implementing continuous improvement projects to reduce product cost, improve product quality, improve process safety and simplify processes to improve compliance. Initiates process manufacturing area change proposals as required.
- Supports Manufacturing aspects of annual product reviews, continued process verification, product/process risk assessments, FMEAs, etc. Minimum of 25% shop floor/unit operation presence is required to successfully support manufacturing.
- Leads technology transfer and implementation of new technologies, equipment, and processes from R&D and other sites, into the Kansas City facility or out to other Catalent sites, as well as between clinical and commercial manufacturing.
- Train and mentor manufacturing product leads and help train manufacturing colleagues on product/processes and equipment technology as required.
- All other duties as assigned.
The Candidate
- Bachelor of Science degree required; preferably in engineering, science or other related technical discipline.
- 7+ years experience in OSD pharmaceutical operations is required. Prefer experience in pharmaceutical production and process engineering.
- Excellent verbal, written, and interpersonal communication skills are essential as this is a client-facing role.
- Understanding of cGMPs, demonstrated leadership, management and technical capabilities preferred.
- Must have demonstrated ability to organize and implement projects that improve the operational effectiveness of product manufacturing.
- Proficient in Microsoft Office Tools.
- Experience in Lean Manufacturing/OpEx and Six Sigma is desired.
Why you should join Catalent
- Career growth with a clear path and regular performance reviews
- Day-one benefits: medical, dental, vision
- 401(k) match, tuition reimbursement, and wellness perks
- Paid time off: 152 hours + 8 holidays
- Inclusive culture with Employee Resource Groups and community initiatives
- Discounts from 900+ merchants via Perkspot
- A mission-driven workplace where your work helps save lives
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.
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.
Senior Manufacturing Product Lead
Position Summary
- Work Schedule: first shift, Monday to Friday
- 100% on-site in Kansas City
Catalent’s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics.
The Role
- Collaborates cross-functionally with Manufacturing, Engineering, Maintenance, EHS and Quality to optimize productivity, safety, product quality and supply reliability for commercial products in compliance with cGMPs.
- Ensures commercial drug product manufacturing is Ready to Execute (RTE): Authors, reviews and approves commercial product manufacturing master batch records, BOMs, equipment recipes and cleaning verification forms as necessary to ensure RTE reliability.
- Partner with commercial clients as required on technical issues affecting their drug product(s). Act as product technical steward on client interactions.
- Provides technical support for process manufacturing areas, including investigation and correction of product/process-related problems and deviations, process troubleshooting and improvements.
- Serves as a subject matter expert during internal audits and regulatory inspections for technical aspects of the drug product process.
- Responsible for identifying, executing and implementing continuous improvement projects to reduce product cost, improve product quality, improve process safety and simplify processes to improve compliance. Initiates process manufacturing area change proposals as required.
- Supports Manufacturing aspects of annual product reviews, continued process verification, product/process risk assessments, FMEAs, etc. Minimum of 25% shop floor/unit operation presence is required to successfully support manufacturing.
- Leads technology transfer and implementation of new technologies, equipment, and processes from R&D and other sites, into the Kansas City facility or out to other Catalent sites, as well as between clinical and commercial manufacturing.
- Train and mentor manufacturing product leads and help train manufacturing colleagues on product/processes and equipment technology as required.
- All other duties as assigned.
The Candidate
- Bachelor of Science degree required; preferably in engineering, science or other related technical discipline.
- 7+ years experience in OSD pharmaceutical operations is required. Prefer experience in pharmaceutical production and process engineering.
- Excellent verbal, written, and interpersonal communication skills are essential as this is a client-facing role.
- Understanding of cGMPs, demonstrated leadership, management and technical capabilities preferred.
- Must have demonstrated ability to organize and implement projects that improve the operational effectiveness of product manufacturing.
- Proficient in Microsoft Office Tools.
- Experience in Lean Manufacturing/OpEx and Six Sigma is desired.
Why you should join Catalent
- Career growth with a clear path and regular performance reviews
- Day-one benefits: medical, dental, vision
- 401(k) match, tuition reimbursement, and wellness perks
- Paid time off: 152 hours + 8 holidays
- Inclusive culture with Employee Resource Groups and community initiatives
- Discounts from 900+ merchants via Perkspot
- A mission-driven workplace where your work helps save lives
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.
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.
See all 33+ Manufacturing at Catalent Pharma Solutions jobs
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Get Access To All JobsTips for Finding Manufacturing Jobs at Catalent Pharma Solutions Jobs
Align your credentials to GMP manufacturing
Catalent's manufacturing roles require demonstrated familiarity with Good Manufacturing Practices. Before applying, document specific GMP experience on your resume with process names, equipment operated, and regulatory frameworks like FDA 21 CFR Part 211, since hiring managers screen for this explicitly.
Target sites with active biologics or CDMO pipelines
Catalent's high-volume hiring tends to cluster around its biologics and drug product sites. Research which facilities have announced capacity expansions or new client contracts, then apply directly to those locations to find roles with the strongest sponsorship urgency.
Understand OPT STEM extension timing for pharma roles
Manufacturing engineer and process scientist roles at Catalent frequently qualify under STEM OPT extension eligible CIP codes. Apply early enough that your 24-month STEM extension covers the full H-1B petition and lottery cycle, giving both you and Catalent a clean sponsorship runway.
Use Migrate Mate to filter verified sponsoring roles
Not every manufacturing listing at Catalent explicitly states visa sponsorship. Use Migrate Mate to browse only the roles where Catalent has a verified sponsorship history, so you spend your applications on positions where the path forward is already established.
Clarify sponsorship scope before accepting an offer
Ask Catalent's recruiter whether the offer covers H-1B filing fees, premium processing, and eventual Green Card sponsorship through PERM. Pharma CDMOs vary on what they cover, and confirming this before signing protects you from unexpected costs or timeline gaps.
Prepare your PERM documentation early for manufacturing titles
Manufacturing roles at Catalent often follow EB-2 or EB-3 Green Card pathways through DOL's PERM labor certification. Gather your foreign degree equivalency evaluations and employment verification letters before your employer initiates PERM, since missing documents are the most common cause of delays.
Manufacturing at Catalent Pharma Solutions jobs are hiring across the US. Find yours.
Find Manufacturing at Catalent Pharma Solutions JobsFrequently Asked Questions
Does Catalent Pharma Solutions sponsor H-1B visas for Manufacturings?
Yes, Catalent Pharma Solutions sponsors H-1B visas for qualifying manufacturing roles. Positions in process engineering, manufacturing sciences, and quality operations are among those most commonly supported. Because the H-1B is subject to an annual lottery, Catalent typically initiates petitions in March for an October 1 start date, so aligning your offer timeline accordingly matters.
How do I apply for Manufacturing jobs at Catalent Pharma Solutions?
You can apply directly through Catalent's careers portal or browse verified sponsorship-eligible listings through Migrate Mate, which filters Catalent manufacturing roles by visa type. Tailor your application to highlight GMP experience, relevant regulatory knowledge, and any specific drug product or biologics exposure, since Catalent's hiring teams screen heavily for site-relevant technical skills.
Which visa types are commonly used for Manufacturing roles at Catalent Pharma Solutions?
Catalent sponsors several visa categories for manufacturing professionals, including H-1B for specialty occupation roles, F-1 OPT and CPT for recent graduates, and TN visas for Canadian and Mexican nationals in qualifying engineering or scientific roles. For longer-term employees, Catalent supports Green Card sponsorship through EB-2 and EB-3 classifications via PERM labor certification filed with the DOL.
What qualifications does Catalent Pharma Solutions expect for Manufacturing roles?
Most manufacturing roles require a bachelor's degree or higher in a relevant field such as chemical engineering, pharmaceutical sciences, biochemistry, or a related discipline. Practical experience with GMP-regulated production environments, validation protocols, or biologics manufacturing is strongly favored. For H-1B sponsorship, your degree must align directly with the specific job duties, so generalist backgrounds without field-specific coursework can complicate the petition.
How do I navigate the sponsorship process timeline for a Manufacturing role at Catalent?
If you're on F-1 OPT, confirm your OPT expiration date before your offer is extended, since Catalent will need enough lead time to file your H-1B petition before your status lapses. USCIS standard processing runs several months, so most candidates use premium processing for a faster decision. For TN status, the process is faster and can often be completed at a port of entry without USCIS filing.
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