Specialist, Manufacturing Support and Documentation Control

Job overview

The Specialist, Manufacturing Support and Documentation Control role is onsite in Pennington, NJ. Compensation is not specified. The role supports Drug Substance and Drug Product manufacturing and works with Manufacturing, Quality, Supply Chain, Warehouse, Engineering, and Validation. The role maintains controlled GMP documentation and helps ensure records and materials are ready to support production schedules. Through document lifecycle control, cross-functional coordination, and continuous improvement, it supports compliant and reliable manufacturing operations.

What you'll do

• Issue, reconcile, maintain, and archive GMP documentation and labels
• create and issue logbooks
• oversee revisions to batch records, protocols, and controlled documents
• scan and file records
• support document management workflows, material staging, SAP reservations, training records, deviations, and change controls
• coordinate documentation and materials with manufacturing and supply chain teams
• support continuous improvement.

What we're looking for

Skills & competencies

beone medicines

manufacturing support

documentation control

gmp documentation

biopharmaceutical manufacturing

batch records

document control

drug substance

drug product

sap

pennington nj

weekend availability

Work arrangement

• Weekend coverage required

Why this role

Requires at least four years of biopharmaceutical manufacturing experience and a bachelor’s degree in science or engineering, or equivalent industry experience. The role may support manufacturing-floor activities as needed and may require off-shift hours and weekends on occasion.

About the employer

BeOne Medicines is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.