Biopharma Production Scheduler & ERP Planner

ADP, Inc.; Branchburg Township (NJ); Hybrid; USD 65,000 - 108,000; Full time

Benefits offered by this job

Paid time off

Medical

Dental

Vision insurance

Life insurance

Retirement savings plan

Wellness programs

Disability benefits

Job summary

Celltrion Branchburg, LLC is seeking an Associate - Production Planner to manage process orders and batch records, and to provide frontline support for timely batch submissions. You will train staff on Veeva usage, handle documentation, and act as SME for the Veeva system in a production environment.

The role requires collaboration with manufacturing, warehouse, and finance, strict safety adherence, and potential hybrid work flexibility. 1–4 years in FDA/ISO manufacturing is expected.

Qualifications

• 1-4 years’ experience in FDA/ISO industry, working in commercial, clinical manufacturing environment.
• Functional expertise in SAP, Veeva, TrackWise, and Microsoft Office.
• Excellent verbal and written communication skills.

Responsibilities

• Request the relevant batch records to document control for manufacturing execution.
• Effectively manage and maintain process orders creation, conversions and releases by adhering to production schedule and cross functional teamwork across different teams.
• Establish effective communication and collaborate with manufacturing, warehouse, operations planning and finance to resolve bottlenecks.
• Monitor, account and report on any non-routine material usages in SAP.
• Check material availability to confirm all required materials are released and available for manufacturing execution.
• Perform recording of raw materials, components, excipients, and quantities used during manufacturing in the ERP system.

Skills

Analytical skills

Attention to detail

Team player

Communication skills

Education

High School Diploma

Bachelor’s degree preferred

Tools

SAP

Veeva

TrackWise

Microsoft Office

Job description

Celltrion Branchburg, LLC is seeking an Associate - Production Planner to manage process orders and batch records, and to provide frontline support for timely batch submissions. You will train staff on Veeva usage, handle documentation, and act as SME for the Veeva system in a production environment.

The role requires collaboration with manufacturing, warehouse, and finance, strict safety adherence, and potential hybrid work flexibility. 1–4 years in FDA/ISO manufacturing is expected.