Supply Chain Associate Visa Sponsorship Jobs in New Jersey
New Jersey's supply chain associate jobs span pharmaceutical giants like Johnson & Johnson and Becton Dickinson in the northern corridor, consumer goods operations near Newark and Elizabeth, and logistics hubs tied to Port Newark. Employers across these industries regularly file for work visa sponsorship, making the state a strong market for international candidates in supply chain roles.
Find Supply Chain Associate JobsOverview
Showing 5 of 101+ Supply Chain Associate Jobs in New Jersey with Visa Sponsorship
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 101+ Supply Chain Associate Jobs in New Jersey with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Supply Chain Associate Jobs in New Jersey with Visa Sponsorship.
Get Access To All JobsTitle: Associate Director, Supply Chain
Date: May 20, 2026
Location: Cranbury, NJ (Commerce Drive)
Company: Sun Pharmaceutical Industries, Inc (USA)
Primary Objective
The Associate Director will support the manufacture of Drug Product (fill finish, device assembly and secondary packaging) of biologics product. Responsible for activities range from tech transfer, technical process studies, process validation activities, data analysis to handing change controls, deviations and troubleshooting. Writing and reviewing of DP/Device Assembly/FG validation-related documents and key CMC sections of regulatory dossiers (different countries) are also required for this position. In addition, also represent and support supply chain team from commercial and clinical supplies of Biologics.
Major Duties/Responsibilities
- Lead and oversee the operational activities at DP/FG/Device Assembly CMO’s; scheduling of batches, commercial manufacturing and testing of DP
- Responsible to achieve on-time in-full manufacturing of DP/FG/Device Assembly in compliance with approved dossiers in collaboration with Quality Assurance, Regulatory Affairs, and Analytical teams
- Serve as DP Subject Matter Expert (SME) on multidisciplinary CMC teams to ensure scientifically driven development and optimization of biological processes
- Review and approve master batch records, change controls, and deviations, CAPA to ensure GMP compliance and operational success
- Preparation and review of documents such as CPV reports, risk assessments, technical reports, validation documents, deviation reports and regulatory modules
- Responsible for Tech Transfer and Process Validation into Commercialization
- Plan and forecast budgets, analyzing variances for production and development testing and execute the day-to-day financial activities in accordance with procedures and contracts.
- Support the supply chain process for clinical and commercial programs to align with functional leaders and senior management on demand and supply plans.
- Coordinates supply activities with Clinical Operations, Technical Operations, Regulatory, Quality Operations, and other departments as necessary to develop optimal supply strategies.
- The candidate will communicate across the organization to ensure key stakeholders are aware of project status, potential risks and their required action plans.
- Supporting post launch market surveillance of the product
- Other duties as assigned
Education
B.E./BTech, MS or Ph.D. degree in (bio) chemical engineering, biotechnology
Professional Experience
- Doctorate degree with 1-3 years of related experience - or - Master's degree and 3-5 years of related experience - or - Bachelor's degree and 5-7 years of direct experience in Biologics Drug Product GMP manufacturing
- Experience in cGMP Biologics Drug Product is a must
- Knowledge of statistical tools like minitab/JMP for data analysis is required
- Knowledge of analytical testing methods and impact on product quality specifications is advantageous.
Skills & Abilities
- Excellent interpersonal and communication, presentation skills
- Excellent organizational and project management skills, work well under pressure
- Ability to diagnose complex issues; develop and implement solutions by collaborating with other teams.
- Ability to influence internal and external stakeholders through scientific justifications
- Ability to thrive in a small group setting with limited administrative support
The presently-anticipated base compensation pay range for this position is $146,500 to $162,500. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
Title: Associate Director, Supply Chain
Date: May 20, 2026
Location: Cranbury, NJ (Commerce Drive)
Company: Sun Pharmaceutical Industries, Inc (USA)
Primary Objective
The Associate Director will support the manufacture of Drug Product (fill finish, device assembly and secondary packaging) of biologics product. Responsible for activities range from tech transfer, technical process studies, process validation activities, data analysis to handing change controls, deviations and troubleshooting. Writing and reviewing of DP/Device Assembly/FG validation-related documents and key CMC sections of regulatory dossiers (different countries) are also required for this position. In addition, also represent and support supply chain team from commercial and clinical supplies of Biologics.
Major Duties/Responsibilities
- Lead and oversee the operational activities at DP/FG/Device Assembly CMO’s; scheduling of batches, commercial manufacturing and testing of DP
- Responsible to achieve on-time in-full manufacturing of DP/FG/Device Assembly in compliance with approved dossiers in collaboration with Quality Assurance, Regulatory Affairs, and Analytical teams
- Serve as DP Subject Matter Expert (SME) on multidisciplinary CMC teams to ensure scientifically driven development and optimization of biological processes
- Review and approve master batch records, change controls, and deviations, CAPA to ensure GMP compliance and operational success
- Preparation and review of documents such as CPV reports, risk assessments, technical reports, validation documents, deviation reports and regulatory modules
- Responsible for Tech Transfer and Process Validation into Commercialization
- Plan and forecast budgets, analyzing variances for production and development testing and execute the day-to-day financial activities in accordance with procedures and contracts.
- Support the supply chain process for clinical and commercial programs to align with functional leaders and senior management on demand and supply plans.
- Coordinates supply activities with Clinical Operations, Technical Operations, Regulatory, Quality Operations, and other departments as necessary to develop optimal supply strategies.
- The candidate will communicate across the organization to ensure key stakeholders are aware of project status, potential risks and their required action plans.
- Supporting post launch market surveillance of the product
- Other duties as assigned
Education
B.E./BTech, MS or Ph.D. degree in (bio) chemical engineering, biotechnology
Professional Experience
- Doctorate degree with 1-3 years of related experience - or - Master's degree and 3-5 years of related experience - or - Bachelor's degree and 5-7 years of direct experience in Biologics Drug Product GMP manufacturing
- Experience in cGMP Biologics Drug Product is a must
- Knowledge of statistical tools like minitab/JMP for data analysis is required
- Knowledge of analytical testing methods and impact on product quality specifications is advantageous.
Skills & Abilities
- Excellent interpersonal and communication, presentation skills
- Excellent organizational and project management skills, work well under pressure
- Ability to diagnose complex issues; develop and implement solutions by collaborating with other teams.
- Ability to influence internal and external stakeholders through scientific justifications
- Ability to thrive in a small group setting with limited administrative support
The presently-anticipated base compensation pay range for this position is $146,500 to $162,500. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
Supply Chain Associate Job Roles in New Jersey
See all 101+ Supply Chain Associate Jobs in New Jersey
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Supply Chain Associate Jobs in New JerseySupply Chain Associate Jobs in New Jersey: Frequently Asked Questions
Which companies sponsor visas for supply chain associates in New Jersey?
Several large employers with significant New Jersey operations have a history of sponsoring work visas for supply chain roles. These include pharmaceutical and life sciences companies such as Johnson & Johnson, Becton Dickinson, and Merck, as well as consumer goods and logistics firms based in the northeastern part of the state. Larger corporations with established HR and legal infrastructure are generally more likely to support the sponsorship process than smaller employers.
Which visa types are most common for supply chain associate roles in New Jersey?
The H-1B visa is the most commonly used visa for supply chain associates in New Jersey, provided the role qualifies as a specialty occupation requiring at least a bachelor's degree in a relevant field such as supply chain management, operations, or industrial engineering. Some candidates on F-1 OPT or STEM OPT also work in these roles while seeking longer-term sponsorship. TN visas are available for Canadian and Mexican nationals in qualifying professional categories.
How to find supply chain associate visa sponsorship jobs in New Jersey?
Migrate Mate is built specifically for international candidates and filters supply chain associate jobs in New Jersey by visa sponsorship willingness, saving you from sorting through postings that won't support your work authorization. You can browse current openings across the state's pharmaceutical, logistics, and consumer goods sectors in one place. Creating an account gives you access to the full list of sponsoring employers actively hiring for these roles.
Which cities in New Jersey have the most supply chain associate sponsorship jobs?
The highest concentration of supply chain associate roles with sponsorship potential is in the northern and central parts of the state. Cities like Newark, Edison, Parsippany, and New Brunswick are strong areas given the density of pharmaceutical headquarters, distribution centers, and corporate offices there. The Port Newark and Elizabeth port area also generates demand in logistics-adjacent supply chain roles, making the northeastern corridor particularly active for international job seekers.
Are there any New Jersey-specific considerations for supply chain associates seeking visa sponsorship?
New Jersey's concentration of life sciences and pharmaceutical employers means many supply chain associate roles require industry-specific knowledge, and employers in regulated industries tend to have formal HR processes that include visa sponsorship. Rutgers University and NJIT produce a pipeline of operations and supply chain graduates familiar to local employers, which can influence hiring preferences. Candidates should confirm that their specific role and degree field meet H-1B specialty occupation requirements, as general operations roles can sometimes face scrutiny during USCIS review.
What is the prevailing wage for sponsored supply chain associate 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.