Looking for W2 Candidates. No C2C

Need a strong technical expertise in Java full stack with project management from pharma domain projects.

Job Description:

Lead and oversee IT initiatives supporting cell therapy digital platforms that drive manufacturing, orchestration, integration, and compliance within regulated pharmaceutical environments-spanning vendor systems such as MES, LIMS, SAP, and scheduling systems.

Key Responsibilities:
Overall 12-17+ years of IT experience and 7+year of experience in technical program management with experience in US pharma, Drug Manufacturing, Cell Therapy and US pharma regulations.
Cross Functional Program Leadership
Coordinate with Digital, Engineering, Quality, Regulatory, QA, and Manufacturing teams.
Experience in personalized or cell therapy manufacturing environments.
Familiarity with digital validation frameworks in CAR-T and related cell therapy platforms.
Computer System Validation (CSV)
Represent Digital in regulatory audits and inspections.
Technical and Architectural Oversight
Engage in technical design/architecture discussions to de-risk validation.
Able to drive cross-functional alignment and clear communication across scientific, operational, IT, and QA/regulatory teams.
Capable of managing vendors, delivering on complex project scopes, milestones, timelines.

Required Technical Expertise:
Programming & Frameworks: React JS, Python, Java, Camunda BPM.
Data & Analytics: SQL, Python, R; Snowflake, Azure Synapse, Databricks;
Cloud Ecosystems: AWS,
Integration: RESTful APIs, Webmethods.