GMP-Driven Database Migration Specialist (Remote)

Nephron Pharmaceuticals Corporation; West Columbia (SC); On-site; USD 90,000 - 150,000; Full time

Job summary

Nephron Pharmaceuticals Corporation in the United States seeks a Database Implementation & Migration Specialist to lead the CMMS data migration from Indy Soft to a Blue Mountain RAM cloud environment, ensuring regulatory alignment.

You will design relational data models, execute ETL, validate data for FDA 21 CFR Part 11/GMP, and develop SOPs plus training for calibration and maintenance staff.

Qualifications

• 5+ years in database development, data engineering, or systems administration in regulated environments.
• Experience migrating data within Life Sciences/Pharma/biotech or advanced manufacturing.
• Hands-on with Indy Soft and Blue Mountain RAM is highly preferred.
• Proficiency with Excel data modeling, VBA, and PowerBI.
• Knowledge of FDA quality and data integrity requirements (IQ/OQ/PQ).

Responsibilities

• Map, extract, transform, and load historical data from Indy Soft to Blue Mountain RAM.
• Align asset tracking hierarchies to Blue Mountain RAM structures.
• Map workflows and scheduling to automated pre-validated routing.
• Ensure data preservation and support IQ/OQ/PQ, electronic signatures, and audit trails.
• Build data-reconciliation models and monitor migration metrics.
• Create SOPs and deliver technical training for staff.
• Develop templates and workflows within the RAM application.

Skills

Relational DB design

Data migration

ETL

Excel modeling

VBA

PowerBI

QA compliance

IQ/OQ/PQ

Data integrity

FDA regulations

Education

Bachelor’s degree in Systems Eng/CS/Engineering

Six Sigma Green Belt

PMP or vendor-certified credentials

Tools

Indy Soft Calibration Management

Blue Mountain RAM

SQL/Relational DB tools

Job description

Nephron Pharmaceuticals Corporation in the United States seeks a Database Implementation & Migration Specialist to lead the CMMS data migration from Indy Soft to a Blue Mountain RAM cloud environment, ensuring regulatory alignment.

You will design relational data models, execute ETL, validate data for FDA 21 CFR Part 11/GMP, and develop SOPs plus training for calibration and maintenance staff.