Ajanta Pharma USA Inc
Supply Chain / DSCSA Analyst
Ajanta Pharma USA Inc. is engaged in the sales and marketing of generic drugs. It is a subsidiary of Ajanta Pharma Limited, a fully integrated pharmaceutical company with global headquarters in Mumbai, India. Over 6,000 employees globally are engaged in developing, manufacturing and marketing of quality finished dosages across 30 countries.
Location: Bridgewater, NJ. This is NOT A REMOTE ROLE. Employee is expected to work from corporate office 3 days a week.
Base pay range: $60,000.00/yr – $70,000.00/yr.
Compensation: $28–$33 per hour ($60,000–$70,000 annualized), plus overtime eligibility. This position is also eligible for participation in the Company’s comprehensive benefits program (medical/dental/vision), PTO, and retirement saving program participation and Company matching.
Essential Job Functions
Support daily DSCSA operations including product serialization, traceability, and exception handling.
Coordinate with internal teams (QA, IT, Logistics) and external partners (CMOs, 3PLs, wholesalers) to ensure accurate product data exchange.
Monitor and investigate DSCSA compliance issues such as “data no product” and “product no data” exceptions.
Ensure accurate and timely submission of T3 data (Transaction Information, Transaction History, and Transaction Statement).
Reconcile all outbound shipments from the 3PL using the middleware system to ensure compliance with DSCSA guidelines.
Maintain records of DSCSA-related activities in compliance with FDA regulations.
Assist with system testing, documentation, and implementation of serialization and verification solutions (e.g., EPCIS, VRS).
Stay updated on evolving FDA DSCSA regulations and industry best practices.
Inputs all inbound shipments into NetSuite.
Manages receipts of product into NetSuite and the 3PL.
Active participant in the S&OP process and monthly S&OP meeting.
Manages any EDI errors between ERP (NetSuite) EDI provider (SPS); including EDI 850, 940, 945, 856.
Works with outside providers (NetSuite, SPS, Tracelink) to troubleshoot any issues.
Participate in audits, inspections, and readiness exercises.
Other Duties
As assigned.
Supervisory Responsibilities None
Education & Experience BS/BA degree from a four-year accredited university or college. A minimum of 2 years experience in the generic manufacturing pharmaceutical industry.
Qualifications
Ability to learn new things quickly and work independently.
Ability to thrive in a dynamic and fast-paced environment.
Ability to prioritize duties and manage multiple projects from start to finish.
Navigation of ERP systems, e.g., NetSuite/Oracle, a plus.
Proficient in Microsoft Office including skills in Excel.
Exceptional attention to detail and excellent organizational skills.
Excellent interpersonal written and verbal communication skills.
Experience in the Generic Pharma preferred.
Must have U.S. work authorization now and in the future. This position is not eligible for employer work authorization sponsorship.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Benefits 401(k), Dental insurance, Vision insurance, Medical insurance.
Seniority Level Entry level
Employment Type Full-time
Job Function Management and Manufacturing
Industries Pharmaceutical Manufacturing
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Location: Bridgewater, NJ. This is NOT A REMOTE ROLE. Employee is expected to work from corporate office 3 days a week.
Base pay range: $60,000.00/yr – $70,000.00/yr.
Compensation: $28–$33 per hour ($60,000–$70,000 annualized), plus overtime eligibility. This position is also eligible for participation in the Company’s comprehensive benefits program (medical/dental/vision), PTO, and retirement saving program participation and Company matching.
Essential Job Functions
Support daily DSCSA operations including product serialization, traceability, and exception handling.
Coordinate with internal teams (QA, IT, Logistics) and external partners (CMOs, 3PLs, wholesalers) to ensure accurate product data exchange.
Monitor and investigate DSCSA compliance issues such as “data no product” and “product no data” exceptions.
Ensure accurate and timely submission of T3 data (Transaction Information, Transaction History, and Transaction Statement).
Reconcile all outbound shipments from the 3PL using the middleware system to ensure compliance with DSCSA guidelines.
Maintain records of DSCSA-related activities in compliance with FDA regulations.
Assist with system testing, documentation, and implementation of serialization and verification solutions (e.g., EPCIS, VRS).
Stay updated on evolving FDA DSCSA regulations and industry best practices.
Inputs all inbound shipments into NetSuite.
Manages receipts of product into NetSuite and the 3PL.
Active participant in the S&OP process and monthly S&OP meeting.
Manages any EDI errors between ERP (NetSuite) EDI provider (SPS); including EDI 850, 940, 945, 856.
Works with outside providers (NetSuite, SPS, Tracelink) to troubleshoot any issues.
Participate in audits, inspections, and readiness exercises.
Other Duties
As assigned.
Supervisory Responsibilities None
Education & Experience BS/BA degree from a four-year accredited university or college. A minimum of 2 years experience in the generic manufacturing pharmaceutical industry.
Qualifications
Ability to learn new things quickly and work independently.
Ability to thrive in a dynamic and fast-paced environment.
Ability to prioritize duties and manage multiple projects from start to finish.
Navigation of ERP systems, e.g., NetSuite/Oracle, a plus.
Proficient in Microsoft Office including skills in Excel.
Exceptional attention to detail and excellent organizational skills.
Excellent interpersonal written and verbal communication skills.
Experience in the Generic Pharma preferred.
Must have U.S. work authorization now and in the future. This position is not eligible for employer work authorization sponsorship.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Benefits 401(k), Dental insurance, Vision insurance, Medical insurance.
Seniority Level Entry level
Employment Type Full-time
Job Function Management and Manufacturing
Industries Pharmaceutical Manufacturing
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