Hikma Pharmaceuticals Visa Sponsorship USA
Hikma Pharmaceuticals is a global generic and branded drug manufacturer with a presence across the U.S., Middle East, and Europe. The company sponsors both work visas and permanent residence pathways, making it a viable target for international candidates pursuing careers in pharmaceuticals and life sciences.
See All Hikma Pharmaceuticals JobsOverview
Showing 5 of 23+ Hikma Pharmaceuticals Visa Sponsorship USA jobs


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?
See all 23+ Hikma Pharmaceuticals Visa Sponsorship USA jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Hikma Pharmaceuticals Visa Sponsorship USA roles.
Get Access To All Jobs
Job Title: Process Supervisor - 3rd Shift Monday - Friday
Location: Cherry Hill, NJ
Job Type: Full-time
Req ID: 10721
About us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Job Purpose
This Process Supervisor role manages shift or multiple shift operations within manufacturing departments. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing decisions. Interprets manufacturing policies, procedures, and programs.
KEY ACCOUNTABILITIES
- Responsible for meeting production requirements, delivering quality products to customers in a timely fashion and cost-efficient manner.
- Identify/prioritize/provide resources to assist the department manager to meet the annual operating plan and budgetary commitments.
- Supervise the daily manufacturing operations across a department or multiple departments.
- Emphasize training and implement control systems on the shift or multiple shifts to eliminate product discrepancies.
- Commit to employee feedback and developmental processes.
- Provide a positive and equitable working environment emphasizing Respect/Responsiveness/Results.
- Support and emphasize the Safety and Quality commitments of the department.
- Make staffing decisions.
- Investigate and resolve disciplinary issues up to and including suspensions and terminations.
- Responsible for driving operational excellence and flawless execution in the areas of cost reduction, discard reduction, annual productivity improvements, inventory turnover, regulatory excellence including exception reduction and internal/external regulatory commitment management, on time delivery and lead time reduction, improving the overall safety of the work environment, leadership development and the ability to create a Lean Manufacturing, total employee involvement workplace.
- Regular and predictable onsite attendance and punctuality.
Qualifications / Experience
- B.S. or equivalent, preferably in a technical discipline, required or 10 yrs. site experience in pharmaceutical injectables manufacturing as an alternative to a 4 year degree.
- 5-7 years experience in all aspects of the manufacturing process required.
Skills
- Ability to manage activities of departments through subordinates who exercise full supervision in terms of cost, methods, and employees.
- Ability to interpret and analyze statistical data and information and financial reports, understand and resolve technical difficulties, interface with internal engineering/technical experts and external technical representatives, manage multiple priorities in a manufacturing plant setting, be resourceful to a large manufacturing department.
- Knowledge of World Class manufacturing methods (Lean), Good Manufacturing Practices, Food Drug and Administration guidelines and process validation.
Compensation:
Salary: $78,000 to $84,000. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
What We Offer:
- Annual performance bonus, commission, and share potential.
- Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute.
- A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries.
- 3 personal days (prorated based on hire date).
- 11 company paid holidays.
- Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits.
- Employee discount program.
- Wellbeing rewards program.
- Safety and Quality is a top organizational priority.
- Career advancement and growth opportunities.
- Tuition reimbursement.
- Paid maternity and parental leave.
- Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma’s Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

Job Title: Process Supervisor - 3rd Shift Monday - Friday
Location: Cherry Hill, NJ
Job Type: Full-time
Req ID: 10721
About us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Job Purpose
This Process Supervisor role manages shift or multiple shift operations within manufacturing departments. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing decisions. Interprets manufacturing policies, procedures, and programs.
KEY ACCOUNTABILITIES
- Responsible for meeting production requirements, delivering quality products to customers in a timely fashion and cost-efficient manner.
- Identify/prioritize/provide resources to assist the department manager to meet the annual operating plan and budgetary commitments.
- Supervise the daily manufacturing operations across a department or multiple departments.
- Emphasize training and implement control systems on the shift or multiple shifts to eliminate product discrepancies.
- Commit to employee feedback and developmental processes.
- Provide a positive and equitable working environment emphasizing Respect/Responsiveness/Results.
- Support and emphasize the Safety and Quality commitments of the department.
- Make staffing decisions.
- Investigate and resolve disciplinary issues up to and including suspensions and terminations.
- Responsible for driving operational excellence and flawless execution in the areas of cost reduction, discard reduction, annual productivity improvements, inventory turnover, regulatory excellence including exception reduction and internal/external regulatory commitment management, on time delivery and lead time reduction, improving the overall safety of the work environment, leadership development and the ability to create a Lean Manufacturing, total employee involvement workplace.
- Regular and predictable onsite attendance and punctuality.
Qualifications / Experience
- B.S. or equivalent, preferably in a technical discipline, required or 10 yrs. site experience in pharmaceutical injectables manufacturing as an alternative to a 4 year degree.
- 5-7 years experience in all aspects of the manufacturing process required.
Skills
- Ability to manage activities of departments through subordinates who exercise full supervision in terms of cost, methods, and employees.
- Ability to interpret and analyze statistical data and information and financial reports, understand and resolve technical difficulties, interface with internal engineering/technical experts and external technical representatives, manage multiple priorities in a manufacturing plant setting, be resourceful to a large manufacturing department.
- Knowledge of World Class manufacturing methods (Lean), Good Manufacturing Practices, Food Drug and Administration guidelines and process validation.
Compensation:
Salary: $78,000 to $84,000. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.
What We Offer:
- Annual performance bonus, commission, and share potential.
- Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute.
- A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries.
- 3 personal days (prorated based on hire date).
- 11 company paid holidays.
- Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits.
- Employee discount program.
- Wellbeing rewards program.
- Safety and Quality is a top organizational priority.
- Career advancement and growth opportunities.
- Tuition reimbursement.
- Paid maternity and parental leave.
- Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma’s Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
Job Roles at Hikma Pharmaceuticals Companies
How to Get Visa Sponsorship in Hikma Pharmaceuticals Visa Sponsorship USA
Target roles in regulatory affairs and drug development
Hikma's core business in generic and branded pharmaceuticals means its highest sponsorship activity tends to cluster in scientific and regulatory roles. Focus your search on positions requiring specialized pharmaceutical or biotech credentials, where visa sponsorship is more commonly extended.
Understand that Hikma sponsors both work visas and Green Cards
Hikma has a track record of sponsoring both H-1B and permanent residence pathways, including EB-2 and EB-3 categories. If long-term U.S. residency is your goal, ask hiring managers directly about their Green Card sponsorship process during interviews.
Position yourself as a specialist, not a generalist
Pharmaceutical companies like Hikma sponsor international talent when the role requires highly specialized knowledge. Candidates with advanced degrees in chemistry, pharmacology, or biomedical sciences, or with deep expertise in regulatory submissions, are better positioned to receive sponsorship consideration.
Prepare for a structured, multi-step hiring process
Large pharmaceutical employers like Hikma typically run multi-round hiring processes involving technical assessments and cross-functional interviews. Starting your application early gives you enough runway to clear each stage before sponsorship paperwork timelines become a concern.
Filter for verified sponsors before applying
Not every company that lists a job will sponsor visas for it. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, saving you from applying to roles where sponsorship is unlikely to be offered regardless of qualifications.
Highlight U.S.-relevant pharmaceutical experience in your application
Hikma operates within strict FDA regulatory frameworks. Candidates who can demonstrate familiarity with U.S. pharmaceutical standards, FDA submission processes, or GMP compliance will stand out and make the business case for sponsorship much easier for hiring teams to approve.
Hikma Pharmaceuticals jobs are hiring across the US. Find yours.
Find Hikma Pharmaceuticals JobsSee all 23+ Hikma Pharmaceuticals jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Hikma Pharmaceuticals roles.
Get Access To All JobsFrequently Asked Questions
Does Hikma Pharmaceuticals sponsor H-1B visas?
Yes, Hikma Pharmaceuticals does sponsor H-1B visas. Sponsorship at Hikma tends to be concentrated in specialized scientific, regulatory, and technical roles where candidates hold advanced qualifications in pharmaceutical or life sciences fields. If you're targeting an H-1B with Hikma, focus on positions that clearly require discipline-specific expertise rather than generalist business or operations roles.
What types of visas does Hikma Pharmaceuticals sponsor?
Hikma Pharmaceuticals sponsors both nonimmigrant and immigrant visa categories, including the H-1B work visa and Green Card pathways through the EB-2 and EB-3 employment-based preference categories. This makes Hikma a meaningful option for international candidates who are thinking beyond short-term work authorization and want a company that can support a longer-term U.S. immigration journey.
Which departments or roles at Hikma Pharmaceuticals are most likely to receive visa sponsorship?
Sponsorship at Hikma is most commonly associated with roles in drug development, regulatory affairs, quality assurance, manufacturing sciences, and research and development. These functions align with Hikma's generic and branded pharmaceutical operations and typically require the kind of specialized academic or professional background that supports a sponsorship petition. General management or administrative roles are less likely to come with sponsorship.
How do I find open sponsored jobs at Hikma Pharmaceuticals?
Migrate Mate is the most efficient way to find roles at companies like Hikma with a verified sponsorship track record. Rather than manually researching which employers actually sponsor and which don't, Migrate Mate lets you filter by sponsorship history so every job you apply for comes from a company with a documented record of supporting international candidates.
How do I improve my chances of getting sponsored at Hikma Pharmaceuticals?
The strongest candidates for sponsorship at Hikma combine advanced qualifications in a pharmaceutical discipline with practical experience that maps directly to FDA-regulated environments. Demonstrating familiarity with regulatory submission processes, GMP standards, or drug formulation development signals to hiring teams that you bring specialized value that justifies the sponsorship investment. Tailoring your resume to reflect U.S. pharmaceutical standards rather than general life sciences experience makes a meaningful difference.
See which Hikma Pharmaceuticals employers are hiring and sponsoring visas right now.
Search Hikma Pharmaceuticals Jobs