Pharma IT Technical Program Manager – Digital Platforms Lead

Cloud Analytics Technologies, LLC; New Jersey; On-site; USD 96,000 - 152,000; Full time

Job summary

CLOUD ANALYTICS TECHNOLOGIES LLC is seeking an IT Technical Program Manager to lead complex pharma IT initiatives in New Jersey. You will drive programs spanning MES, LIMS, SAP, and scheduling systems, ensuring GxP compliance and CSV readiness for FDA-regulated environments.

The role requires deep experience in US pharma manufacturing, strong cross‑functional leadership, and the ability to manage vendor relationships and regulatory audits while delivering on schedule and budget.

Qualifications

• 15+ years IT experience with 7+ years in technical program management in pharma.
• Deep understanding of US pharma manufacturing and regulatory requirements.
• Proven ability to lead cross-functional teams across IT, QA, and manufacturing.
• Experience with vendor management and regulatory readiness activities.
• Familiar with CSV and 21 CFR Part 11 compliance in digital systems.

Responsibilities

• Lead IT programs spanning MES, LIMS, SAP, and scheduling systems.
• Drive validation strategies and CSV planning across complex platforms.
• Ensure GxP compliance and inspection readiness for FDA-regulated environments.
• Coordinate with Digital, Engineering, Quality, Regulatory, and Manufacturing teams.
• Manage vendors and oversee milestones, risks, and timelines.

Skills

PM leadership

Pharma domain expertise

GxP compliance

CSV (Computer System Validation)

Vendor management

Regulatory audits

Cross-functional collaboration

System integration

SAP familiarity

Tools

MES

LIMS

SAP

Scheduler

Control systems

mINT Engine

Job description

CLOUD ANALYTICS TECHNOLOGIES LLC is seeking an IT Technical Program Manager to lead complex pharma IT initiatives in New Jersey. You will drive programs spanning MES, LIMS, SAP, and scheduling systems, ensuring GxP compliance and CSV readiness for FDA-regulated environments.

The role requires deep experience in US pharma manufacturing, strong cross‑functional leadership, and the ability to manage vendor relationships and regulatory audits while delivering on schedule and budget.