Specialist, Manufacturing Support and Documentation Control

BeOne Medicines USA; Hopewell (VA); On-site; USD 70,000 - 110,000; Full time

Job summary

BeOne Medicines USA seeks a Manufacturing Support and Documentation Control Specialist to maintain GMP records for Drug Substance and Drug Product, issuing, reconciling, and archiving master batch records, SOPs, work instructions, and labels. The role collaborates with Manufacturing, Quality, Supply Chain, Warehouse, Engineering, and Validation to ensure timely documentation for production.

Candidates should have at least four years in biopharmaceutical manufacturing, strong GMP document-control

Qualifications

• 4+ years of biopharmaceutical manufacturing experience.
• GMP documentation and document-control experience.
• Excellent organizational skills and attention to detail.
• Ability to manage multiple priorities and time-sensitive activities.
• Strong written and verbal communication.
• Experience working cross-functionally with Manufacturing, Quality, Supply Chain and Warehouse.
• Proficiency with Microsoft Office; familiarity with SAP and QMS systems.

Responsibilities

• Issuance of batch-related documentation and labels for GMP manufacturing.
• Reconcile GMP documentation per lifecycle requirements.
• Create and issue GMP logbooks/notebooks.
• Store and archive GMP documents and batch records.
• Perform tasks in line with safety, quality systems and cGMP requirements.
• Drive continuous improvement and support document management operations.
• Oversee revision of batch records and control documents.
• Coordinate documentation tasks across DS, DP, QA, and Warehouse.

Skills

Biopharmaceutical manufacturing

GMP documentation

Document-control practices

Organizational skills

Time management

Cross-functional collaboration

Written and verbal communication

Education

Bachelor's Degree: Science / Engineering or equivalent

Tools

SAP

QMS systems

Microsoft Office

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

Manufacturing Support and Documentation Control Specialist

The Manufacturing Support and Documentation Control Specialist provides day-to-day documentation and operational support to Drug Substance and Drug Product manufacturing. The role is responsible for the issuance, reconciliation, maintenance, and archival of GMP documentation, including master batch records, SOPs, work instructions, forms, labels, logbooks, validation protocols, and related manufacturing records.

The Specialist partners closely with Manufacturing, Quality, Supply Chain, Warehouse, Engineering, and Validation to ensure documentation and materials are available to support production schedules. The role also supports document-control workflows, material staging, SAP reservations, training records, deviations, change controls, and continuous improvement activities while ensuring compliance with cGMP requirements and established quality systems.

Required Skills/Attributes:

• A minimum of 4 years biopharmaceutical manufacturing experience.
• Strong knowledge of GMP documentation and document-control practices.
• Excellent organizational skills and attention to detail-
• Ability to manage multiple priorities and time-sensitive manufacturing activities.
• Strong written and verbal communication skills.
• Experience working cross-functionally with Manufacturing, Quality, Supply Chain, and Warehouse.
• Proficiency with Microsoft Office and familiarity with SAP/QMS systems.

Education Required:

• Bachelor's Degree: Science / Engineering or equivalent experience in biopharmaceutical industry.

Responsibilities:

• Issuance of batch related documentation and labels in support of GMP manufacturing.
• Reconcile GMP documentation following document lifecycle requirements.
• Creation and issuance of GMP logbooks/notebooks.
• Responsible for storage and archival of GMP documents and batch related records.
• Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
• Drive continuous improvement.
• Support Document Management Operations team.
• Oversee revision of Batch record, protocol and other control documents.
• Scan and file documents.
• Supporting project tasks.
• Processing controlled documentation within applicable system.
• Format controlled records and perform accurate data entry in accordance with established documentation standards.
• Advising and responding to queries on document status by interfacing with operation management.
• Prepare, organize, and maintain documentation in accordance with established procedures and cGMP requirements.
• Assist departments with equipment and system documentation. Coordinate system implementation and prepare documentation as necessary.
• Identify specific process improvement as needed and provide recommendations concerning established workflows.
• Work directly with Document Management, Drug Substance, Drug Product, Warehouse, and various Quality organizations.
• Maintain close collaboration with QA, QC, DP, DS and WH operations.
• Managing workflows and metrics for manufacturing areas.

Key Relationships:

• Must attend both the DS and DP, morning huddles.
• Works in a collaborative team setting with quality counterparts that include Manufacturing Operations, Engineering and Validation, Quality Control, Quality Assurance Manufacturing, Supply Chain and Warehouse.
• Manage all Turn-Over-Packages (TOP) and Commissioning Packages from HPW site projects.
• Maintain open communication with management, co-workers, customers, and counterpart staff in other sites as needed.
• Work with Supply Chain to coordinate the manufacturing schedule to support the batch records, labels and forms requirements prior to the start of production.

Production Support

The position will be trained and may also support the following on the manufacturing floor areas as needed basis:

• Drug Substance Area: Master Batch Records, Logbooks, Forms, Labels etc. are all stored in the designated area on the manufacturing floor at least 2 days prior to the production run. Material Staging and room readiness.
• Drug Product: Master Batch Records, Logbooks, Forms, Labels etc. are all stored in the designated area on the manufacturing floor at least 2 days prior to the production run.
• Warehouse: Weigh and dispense Documentation and SAP reservation, Materials readiness prior to campaign start.

Document Management

• Workflow and process alignment for all documentation issuances including labels, Master batch records, SOPs, Work instructions, Forms, etc.

Physical Requirements :

• Must be able to stand for long periods, up to 8 to 12 hours/day.
• Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently.
• Must be able to work scheduled 40 hours with the ability to work overtime as needed.