Catalent Pharma Solutions Green Card Visa Sponsorship Jobs USA
Catalent Pharma Solutions sponsors Green Cards for science and research professionals, particularly in drug development, manufacturing, and quality assurance. The company has an established track record of supporting employees through permanent residency, making it a credible long-term option for international scientists and engineers building careers in the U.S.
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- Shift: Monday – Friday 8am – 4:30pm
- 100% on-site
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The role:
- Supervise and manage various method development, method evaluation/feasibility, method transfers, method verifications, qualifications and validations, stability study and adhoc sample testing in Molecular and Cellular Biology.
- Plan, prioritize, organize, and execute the conduct of analytical work within the Molecular and Cellular Biology Laboratory in accordance with the requirements of the client contract and/or technical agreement.
- Serve as back up Project Technical Lead and could also serve as Technical Lead on projects pertaining to Molecular and Cellular Biology.
- Manage and lead computer system validation activities, as required. Ensure various instruments/Equipment in the group are in compliant status.
- Ensure cGMP practices are implemented and followed by the group and self.
- Assure the integrity and quality of analytical data produced by ensuring staff are adhering to all relevant in-house and client SOPs and methodologies and following the requirements of GMP.
- Monitor and manage projects and maintain project timelines and budget.
- Communicate effectively with clients, auditors, peers, and Directors to facilitate the smooth conduct of project activities.
The candidate:
- Bachelor’s degree: >10 years of relevant experience in department specific techniques with more than 8 years of management experience preferred or based on performance at Catalent, OR
- Master’s degree: >8 years of relevant experience in department specific techniques with more than 6 years of management experience preferred or based on performance at Catalent, OR
- Doctorate Degree: >6 years of relevant experience in department specific techniques with more than 4 year of management experience preferred or based on performance at Catalent.
- Applies knowledge of the principles, theories, and concepts applicable to a wide range of work in a discipline (e.g., Biology, Chemistry, Biochemistry) and broad knowledge of principles and concepts in other disciplines.
- In-depth knowledge in instrumentation, theory, data interpretation and applications in at least one technical area. Can assess new technologies and their impact on Catalent offerings.
- Experienced in most aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones.
- Excellent written and verbal communications skills with internal and external customers, colleagues, and supervisor.
- Ability to communicate complex technical information to non-technical audiences.
- Able to lead difficult discussions with customers and drive the to an acceptable resolution.
Why you should join Catalent:
- Competitive medical benefits and 401K
- 152 hours PTO + 8 Paid Holidays
- Dynamic, fast-paced work environment
- Opportunity to work on Continuous Improvement Processes
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.
Position Summary
- Shift: Monday – Friday 8am – 4:30pm
- 100% on-site
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The role:
- Supervise and manage various method development, method evaluation/feasibility, method transfers, method verifications, qualifications and validations, stability study and adhoc sample testing in Molecular and Cellular Biology.
- Plan, prioritize, organize, and execute the conduct of analytical work within the Molecular and Cellular Biology Laboratory in accordance with the requirements of the client contract and/or technical agreement.
- Serve as back up Project Technical Lead and could also serve as Technical Lead on projects pertaining to Molecular and Cellular Biology.
- Manage and lead computer system validation activities, as required. Ensure various instruments/Equipment in the group are in compliant status.
- Ensure cGMP practices are implemented and followed by the group and self.
- Assure the integrity and quality of analytical data produced by ensuring staff are adhering to all relevant in-house and client SOPs and methodologies and following the requirements of GMP.
- Monitor and manage projects and maintain project timelines and budget.
- Communicate effectively with clients, auditors, peers, and Directors to facilitate the smooth conduct of project activities.
The candidate:
- Bachelor’s degree: >10 years of relevant experience in department specific techniques with more than 8 years of management experience preferred or based on performance at Catalent, OR
- Master’s degree: >8 years of relevant experience in department specific techniques with more than 6 years of management experience preferred or based on performance at Catalent, OR
- Doctorate Degree: >6 years of relevant experience in department specific techniques with more than 4 year of management experience preferred or based on performance at Catalent.
- Applies knowledge of the principles, theories, and concepts applicable to a wide range of work in a discipline (e.g., Biology, Chemistry, Biochemistry) and broad knowledge of principles and concepts in other disciplines.
- In-depth knowledge in instrumentation, theory, data interpretation and applications in at least one technical area. Can assess new technologies and their impact on Catalent offerings.
- Experienced in most aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones.
- Excellent written and verbal communications skills with internal and external customers, colleagues, and supervisor.
- Ability to communicate complex technical information to non-technical audiences.
- Able to lead difficult discussions with customers and drive the to an acceptable resolution.
Why you should join Catalent:
- Competitive medical benefits and 401K
- 152 hours PTO + 8 Paid Holidays
- Dynamic, fast-paced work environment
- Opportunity to work on Continuous Improvement Processes
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.
Job Roles at Catalent Pharma Solutions
How to Get Visa Sponsorship in Catalent Pharma Solutions Green Card Visa Sponsorship Jobs USA
Target roles with clear degree requirements
Green Card sponsorship at Catalent typically follows specialty occupation roles in pharmaceutical sciences, biotech, and engineering. Focus your applications on positions requiring a specific degree field, as these map cleanly to EB-2 and EB-3 eligibility criteria.
Understand the PERM labor certification process
Catalent's Green Card pathway usually begins with PERM, where the Department of Labor certifies no qualified U.S. workers are available. Expect your employer to conduct a formal recruitment process before filing, which can take several months to complete.
Ask about sponsorship timelines during the offer stage
Catalent's HR and immigration teams handle Green Card filings internally and through outside counsel. Raising sponsorship expectations early, during offer negotiation rather than after starting, sets clearer expectations and helps you plan around priority date backlogs.
Position yourself in manufacturing and R&D departments
Science and research roles in drug manufacturing, analytical chemistry, and process development are among the most common Green Card pathways at Catalent. These departments have consistent hiring volume, which correlates with more predictable sponsorship activity.
Use Migrate Mate to identify verified sponsorship roles
Finding companies with real Green Card sponsorship history takes more than reading job descriptions. Migrate Mate surfaces verified sponsors so you can filter by actual sponsorship history, helping you prioritize Catalent openings over companies that only claim to sponsor.
Account for priority date wait times by country of birth
If you were born in India or China, EB-2 and EB-3 priority dates can mean multi-year waits even after Catalent files your petition. Factor this into your career planning and ask your immigration attorney about EB-1 eligibility if your research credentials qualify.
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Get Access To All JobsFrequently Asked Questions
Does Catalent Pharma Solutions sponsor Green Card visas?
Yes, Catalent Pharma Solutions sponsors Green Card visas for qualifying employees in science, research, and engineering roles. The company has a documented history of filing permanent residency petitions, particularly through the EB-2 and EB-3 employment-based categories. Sponsorship is typically offered after a period of employment, not at the point of hire.
Which roles and departments at Catalent Pharma Solutions are most likely to receive Green Card sponsorship?
Roles in pharmaceutical sciences, biotech manufacturing, process development, analytical chemistry, and quality assurance are the most common pathways for Green Card sponsorship at Catalent. These positions require specialized degrees and align well with PERM specialty occupation requirements. Research and development scientists at the senior level are also strong candidates.
How does the Green Card application process work at Catalent Pharma Solutions?
Catalent typically manages Green Card filings through outside immigration counsel. The process begins with PERM labor certification, where the Department of Labor verifies no qualified U.S. workers are available. Once certified, Catalent files an I-140 immigrant petition. After approval, you either adjust status in the U.S. or complete consular processing abroad.
How long does it take to get a Green Card through Catalent Pharma Solutions?
The timeline depends on your visa category, country of birth, and current priority date backlogs. PERM certification alone can take six months to over a year. For applicants born in oversubscribed countries like India or China, EB-2 and EB-3 wait times can extend significantly beyond the initial petition approval. Consult an immigration attorney for a projection specific to your situation.
How do I find open Green Card sponsorship jobs at Catalent Pharma Solutions?
Job listings rarely state Green Card sponsorship explicitly, which makes it hard to know which openings are real opportunities. Migrate Mate aggregates roles from verified sponsors like Catalent and filters by sponsorship type, so you can search specifically for Green Card-eligible positions rather than guessing from job descriptions. Focus on science and manufacturing roles with clear degree requirements.
What is the prevailing wage for Green Card sponsorship at Catalent Pharma Solutions?
Employers sponsoring a Green Card through the PERM labor certification process must pay at least the prevailing wage for the role. The Department of Labor determines this rate based on the specific job title, location, and experience level. The prevailing wage is locked in during the PERM filing and applies through the entire Green Card process. You can look up current rates using the DOL's OFLC Wage Search tool.
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