Biotech & Pharma Visa Sponsorship Jobs in New Jersey
New Jersey's biotech and pharmaceutical industry offers extensive visa sponsorship opportunities, particularly in the Princeton-New Brunswick corridor. Major employers like Johnson & Johnson, Merck, and Bristol Myers Squibb actively sponsor H-1B visa, L-1, and O-1 visas for research scientists, clinical development specialists, and regulatory affairs professionals.
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Job
Location: Cherry Hill, NJ
Job Type: Full-time
Req ID: 9349
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.
KEY RESPONSIBILITIES:
- Regular and predictable onsite attendance and punctuality.
- Sets up & operates equipment such as scales, mixers, pumps, CIP units, tanks and material handling equipment.
- Maintains accurate records, i.e., log books, raw material inventories, reconciliations and batch records.
- Moves raw material as required for mixing, weighing and storage.
- Weighs all chemicals to prepare cleaning solution batches and on a limited basis, production batches designated by the department.
- Performs acid/base pH adjustments as required by batch or as instructed by QA Lab.
- Transfers finished batches to specified area for further processing.
- Adheres strictly to cGMPs and SOPs to ensure the quality and integrity of products.
- Performs clean-up of equipment and rooms as necessary.
- Collects samples, performs other quality checks as necessary.
- Performs preventive maintenance tasks on compounding equipment, such as tanks, mixers and pumps as required or as instructed by supervisor or designee.
- Refers process issues to supervisor or designee.
- Informs supervisor of maintenance and/or safety issues.
- Works overtime with short notice when production requires.
- Under supervision, weighs specified quantities and follows formulation procedures in the preparation of bulk solutions.
- The incumbent may perform other duties as assigned by management personnel.
QUALIFICATIONS
Minimum: High School Diploma with 1 year of experience working in a cGMP facility
Preferred: Associates Degree in Science or Equivalent
Experience
- Minimum: 1-year of working in a cGMP Facility or 1-year Pharmaceutical liquid batching experience with a High School diploma, or 2 years of other batching experience or 2 years of practical laboratory experience with an Associate or Bachelor degree.
- Good oral and written communication skills are essential.
- Must be able to document process issues in a clean, concise manner in accordance with cGMPs and SOPs.
- Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
- Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form.
- Must be able to read and understand complex formulation procedures.
- Ability to deal with problems involving several concrete variables in standardized situations.
- Ability to examine problem areas and make recommendations for corrective action.
- Must be able to comprehend and follow all applicable SOPs.
- Heavy continuous exertion.
- Movement and weighing of heavy containers up to 100 lbs., lifts 45 – 50 lbs. 25 – 50% of time.
- Movement of portable tanks may require the use of a power pusher which requires 20/40 distance vision and ability to pass a whisper test (or have no worse than 40 dBA in the better ear).
- Must be able to stand for long periods of time.
- Must be able to climb ladders and platforms to dispense chemicals.
- Must be able to wear required PPE.
- Work involves exposure to raw materials which requires special handling and protective equipment.
- Operators are exposed to raw materials 80% of the time.
- Must work in compounding suites wearing company issued frock (long laboratory coat), hood, and boots.
- Must wear PAPRs and successfully complete and pass pulmonary function testing.
- The noise level is moderate to loud in CIP Washrooms; use of hearing protection may be required.
- The use of sanitizing agents to clean the compounding rooms may be moderately disagreeable.
Compensation:
Hourly Rate: $25.50 per hour. 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 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.
Location: Cherry Hill, NJ, US, 08003
Nearest Major Market: Philadelphia

Job
Location: Cherry Hill, NJ
Job Type: Full-time
Req ID: 9349
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.
KEY RESPONSIBILITIES:
- Regular and predictable onsite attendance and punctuality.
- Sets up & operates equipment such as scales, mixers, pumps, CIP units, tanks and material handling equipment.
- Maintains accurate records, i.e., log books, raw material inventories, reconciliations and batch records.
- Moves raw material as required for mixing, weighing and storage.
- Weighs all chemicals to prepare cleaning solution batches and on a limited basis, production batches designated by the department.
- Performs acid/base pH adjustments as required by batch or as instructed by QA Lab.
- Transfers finished batches to specified area for further processing.
- Adheres strictly to cGMPs and SOPs to ensure the quality and integrity of products.
- Performs clean-up of equipment and rooms as necessary.
- Collects samples, performs other quality checks as necessary.
- Performs preventive maintenance tasks on compounding equipment, such as tanks, mixers and pumps as required or as instructed by supervisor or designee.
- Refers process issues to supervisor or designee.
- Informs supervisor of maintenance and/or safety issues.
- Works overtime with short notice when production requires.
- Under supervision, weighs specified quantities and follows formulation procedures in the preparation of bulk solutions.
- The incumbent may perform other duties as assigned by management personnel.
QUALIFICATIONS
Minimum: High School Diploma with 1 year of experience working in a cGMP facility
Preferred: Associates Degree in Science or Equivalent
Experience
- Minimum: 1-year of working in a cGMP Facility or 1-year Pharmaceutical liquid batching experience with a High School diploma, or 2 years of other batching experience or 2 years of practical laboratory experience with an Associate or Bachelor degree.
- Good oral and written communication skills are essential.
- Must be able to document process issues in a clean, concise manner in accordance with cGMPs and SOPs.
- Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
- Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form.
- Must be able to read and understand complex formulation procedures.
- Ability to deal with problems involving several concrete variables in standardized situations.
- Ability to examine problem areas and make recommendations for corrective action.
- Must be able to comprehend and follow all applicable SOPs.
- Heavy continuous exertion.
- Movement and weighing of heavy containers up to 100 lbs., lifts 45 – 50 lbs. 25 – 50% of time.
- Movement of portable tanks may require the use of a power pusher which requires 20/40 distance vision and ability to pass a whisper test (or have no worse than 40 dBA in the better ear).
- Must be able to stand for long periods of time.
- Must be able to climb ladders and platforms to dispense chemicals.
- Must be able to wear required PPE.
- Work involves exposure to raw materials which requires special handling and protective equipment.
- Operators are exposed to raw materials 80% of the time.
- Must work in compounding suites wearing company issued frock (long laboratory coat), hood, and boots.
- Must wear PAPRs and successfully complete and pass pulmonary function testing.
- The noise level is moderate to loud in CIP Washrooms; use of hearing protection may be required.
- The use of sanitizing agents to clean the compounding rooms may be moderately disagreeable.
Compensation:
Hourly Rate: $25.50 per hour. 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 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.
Location: Cherry Hill, NJ, US, 08003
Nearest Major Market: Philadelphia
Biotech & Pharma Job Roles in New Jersey
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Search Biotech & Pharma Jobs in New JerseyBiotech & Pharma Jobs in New Jersey: Frequently Asked Questions
Which biotech & pharma companies sponsor visas in New Jersey?
Major sponsors include Johnson & Johnson (New Brunswick), Merck (Rahway), Bristol Myers Squibb (Princeton), Celgene (Summit), and Novartis (East Hanover). These companies regularly file H-1B petitions for research scientists, clinical research associates, biostatisticians, and regulatory affairs specialists. Smaller biotechs like Acelity and Catalent also sponsor visas for specialized roles in drug development and manufacturing.
How to find biotech & pharma visa sponsorship jobs in New Jersey?
Use Migrate Mate to search specifically for biotech and pharmaceutical positions with visa sponsorship in New Jersey. The platform filters jobs by industry and location, showing which employers actively sponsor work visas. Focus on research hubs around Princeton, New Brunswick, and Summit where most pharmaceutical companies are concentrated and have the highest demand for international talent.
Which visa types are most common for biotech & pharma roles in New Jersey?
H-1B visas dominate for research scientists, clinical data managers, and regulatory affairs roles requiring specialized knowledge. L-1 visas are common for transferees from international pharmaceutical companies. O-1 visas are used for senior researchers with distinguished careers in drug development. TN visas apply to Canadian and Mexican nationals in qualifying scientific positions.
Which cities in New Jersey have the most biotech & pharma sponsorship jobs?
Princeton leads with companies like Bristol Myers Squibb and multiple biotech startups. New Brunswick hosts Johnson & Johnson's headquarters and research facilities. Rahway houses Merck's major operations. Summit, East Hanover, and Bridgewater also concentrate pharmaceutical companies. The I-287 corridor from Princeton to Bridgewater forms the state's primary pharmaceutical belt with the highest visa sponsorship activity.
What are the prevailing wage requirements for biotech roles in New Jersey?
New Jersey's biotech prevailing wages reflect the state's high cost of living and concentration of pharmaceutical headquarters. Research scientist positions typically require Level 2-3 prevailing wages, while senior roles and specialized positions like clinical development or regulatory affairs often qualify for Level 3-4 wages. The Newark-Jersey City metro area has higher wage requirements than southern New Jersey.
What is the prevailing wage for sponsored biotech & pharma jobs in New Jersey?
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.
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