Java Technical Project Manager (Pharma Domain) _ New Jersey (Day1 onsite)

Overview

On Site
Depends on Experience
Accepts corp to corp applications
Contract - Independent
Contract - W2
Contract - 12 Month(s)

Skills

Java
Python
Reactjs
SQL
Pharma

Job Details

Requirement details:

Job Title: Java Technical Project Manager (Pharma Domain)

Location: New Jersey (Day1 onsite)

Duration : 12+ Months

Role Overview: 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.

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, Web methods

Key Responsibilities:

Overall 12-17+ years of IT experience and 7+year of experience in technical program management with deep experience in US pharma, Drug Manufacturing, Cell Therapy and US pharma regulations.

Cross Functional Program Leadership

Manage end-to-end IT programs (e.g., MES/LIMS/SAP integrations, scheduler systems, orchestration platforms).

Coordinate with Digital, Engineering, Quality, Regulatory, QA, and Manufacturing teams.

Strong knowledge of GxP regulations, validation lifecycle, and digital manufacturing system landscapes.

Experience with MES, LIMS, SAP, Scheduler, Control systems, integration architectures.

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)

Develop validation strategy and execute CSV planning across complex digital systems.

Embed GxP (21 CFR Part 11, Annex 11) requirements early during design.

Regulatory Readiness & Inspection Support

Ensure platforms are inspection-ready for BLA submissions and manufacturing transitions.

Represent Digital in regulatory audits and inspections.

Technical and Architectural Oversight

Engage in technical design/architecture discussions to de-risk validation.

Ensure integration readiness across systems (e.g., mINT Engine, Scheduler, Control Tower).

Validation Deliverables Management

Develop/maintain CSV artifacts: plans, risk assessments, URS, protocols, test scripts, trace matrices, validation reports

Business Engagement & Leadership

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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.