IT Technical Manager (Pharma DomainJava & FE background)
Share
Job Location:
New Milford, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
3 days ago
Vacancies:
1 Vacancy
Job Summary
Job Role: IT Technical Manager (Pharma Domain/Java & FE background)
Location: New Jersey (Hybrid ; 3days onsite) (Need Locals Only)
Location: New Jersey (Hybrid ; 3days onsite) (Need Locals Only)
Long Term Contract
Looking for W2 Candidates. No C2C
Need a strong technical expertise in Java full stack with project management from pharma domain projects.
Job Description:
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 7year 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.
Key Responsibilities:
Overall 12-17 years of IT experience and 7year 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.
Best Regards:
Kesav N
Phone: 1-
Email:
Kesav N
Phone: 1-
Email:
Key Skills
- Corporate Accounting
- Facilities Management
- Account Development
- Accountancy
- Jdbc
- ITI
