GMP Operations & Data Specialist (SAP/QA)

Granules Pharmaceuticals, Inc.; Chantilly (VA); On-site; USD 50,000 - 65,000; Full time

Job summary

Granules Pharmaceuticals, Inc. in Chantilly, VA is seeking an Operations Associate to support warehouse and manufacturing processes, uphold cGMP standards, maintain accurate documentation, and drive process optimization.

You will manage SAP master data, participate in automation initiatives and GMP equipment validation, ensure data integrity in reports, and collaborate across teams to sustain regulatory compliance and efficient production.

Qualifications

• Bachelor's degree required; 2+ years in a cGMP-regulated environment preferred.
• Experience writing and maintaining cGMP documentation.
• Experience with materials receipt and storage; strong data analysis skills.

Responsibilities

• Maintain awareness of new data analysis methods for inventory control.
• Prepare cycle count reports and publish findings.
• Document changes and issues in the change control system.
• Create and manage SAP master data (BOM, Material Master, Production versions, etc.).
• Assist in SAP PP/MM modules and data management tasks.
• Support automation initiatives and participate in GMP equipment validation.

Skills

Data analysis

Inventory control

Cross-functional collaboration

Communication skills

Documentation

DEA compliance

cGMP compliance

Education

Bachelor's degree in Healthcare informatics or scientific discipline

Tools

SAP

BMRAM

Job description

Granules Pharmaceuticals, Inc. in Chantilly, VA is seeking an Operations Associate to support warehouse and manufacturing processes, uphold cGMP standards, maintain accurate documentation, and drive process optimization.

You will manage SAP master data, participate in automation initiatives and GMP equipment validation, ensure data integrity in reports, and collaborate across teams to sustain regulatory compliance and efficient production.