IT Technical Program Manager (Java/Pharma Domain) at QUANTUM TECHNOLOGIES LLC

Job description

body> Job Description Job Overview • Job ID: J52578 • Job Title: IT Technical Program Manager (Java/Pharma Domain) • Location: New Jersey, NJ • Duration: 12 Months + Extension • Hourly Rate: Depending on Experience (DOE) • Work Authorization: US Citizen, Green Card, OPT-EAD, CPT, H-1B, H4-EAD, L2-EAD, GC-EAD • Client: To Be Discussed Later • Employment Type: W-2, 1099, C2C View All Jobs Similar Jobs • Java Developer - 423 W WHEATLAND RD, SUITE 103C, DUNCANVILLE, TX 75116 • Oracle HCM Cloud Technical Consultant - Kansas, KY • Project Manager - West Virginia, WV • Senior Project Manager - White Plains, NY • IT Project Manager - Tallahassee, FL 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. Key Responsibilities: • Overall 15-17+ 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. 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. Thanks & Regards Apply Now Equal Opportunity Employer QUANTUM TECHNOLOGIES LLC is an equal opportunity employer inclusive of female, minority, disability and veterans, (M/F/D/V). Hiring, promotion, transfer, compensation, benefits, discipline, termination and all other employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, age, disability, national origin, citizenship/immigration status, veteran status or any other protected status. QUANTUM TECHNOLOGIES LLC will not make any posting or employment decision that does not comply with applicable laws relating to labor and employment, equal opportunity, employment eligibility requirements or related matters. Nor will QUANTUM TECHNOLOGIES LLC require in a posting or otherwise U.S. citizenship or lawful permanent residency in the U.S. as a condition of employment except as necessary to comply with law, regulation, executive order, or federal, state, or local government contract

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Job Overview
IT Technical Program Manager (Java/Pharma Domain)
New Jersey, NJ
12 Months + Extension
Depending on Experience (DOE)
US Citizen, Green Card, OPT-EAD, CPT, H-1B,
To Be Discussed Later
View All Jobs
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IT Project Manager - Tallahassee, FL
Overall 15-17+ 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.

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