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Manufacturing Execution Systems; MES Project Manager

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: Johnson & Johnson Innovative Medicine
Full Time position
Listed on 2026-03-08
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Data Analyst
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Execution Systems (MES) Project Manager

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function

Supply Chain Engineering

Job Sub Function

Automation Engineering

Job Category

People Leader

All Job Posting Locations

Raritan, New Jersey, United States of America

Job Description About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

We are searching for the best talent for a Manufacturing Execution Systems (MES) Project Manager to join our team. This is an onsite position located in Raritan, NJ.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality and reliable supply of our cell therapy products? Apply today for this exciting opportunity to be part of the #CAR‑T team!

Johnson & Johnson Innovative Medicines and Legend Biotech have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T‑cell therapy for BCMA. This strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR‑T platform treatment.

Overview

We are seeking a Manufacturing Execution Systems (MES) Project Manager to support MES delivery, integrations, and validation at the Raritan CAR‑T manufacturing site. This is a hands‑on, project‑focused role ideal for a candidate with 5–7 years of MES/automation experience in regulated pharma/biotech environments. The MES Project Manager will plan and execute MES projects, coordinate vendors and site stakeholders, support CSV activities, and drive successful go‑lives that maintain compliance and enable on‑time patient product delivery.

Key Responsibilities
  • Manage end‑to‑end MES project activities for site initiatives: requirements gathering, functional specifications, vendor coordination, scheduling, risk mitigation, and delivery to scope and budget.
  • Coordinate FAT/SAT, commissioning, and go‑live activities with vendors, IT, manufacturing, and quality and validation teams.
  • Support CSV activities: develop or execute test scripts, assist with IQ/OQ/PQ documentation, maintain trace matrices, and close validation items.
  • Translate operational and quality requirements into MES user stories/functional requirements and acceptance criteria.
  • Work hands‑on with system integrators and site engineers to configure, test, and troubleshoot MES integrations with various systems (LIMS/QC, ERP (SAP), PLC).
  • Create and maintain project plans, status reports, risk logs, and change control documentation; communicate progress and escalation items to business partners.
  • Support creation and delivery of training materials, SOPs, and go‑live support to ensure effective user adoption.
  • Participate in root cause investigations for MES incidents and support corrective actions (CAPA) and continuous improvement efforts.
  • Ensure project and system activities align to GMP, data integrity (ALCOA+), and 21 CFR Part 11 / EMA Annex 11 expectations; elevate compliance concerns to Quality.
  • Support site MES maintenance and minor enhancements as part of a broader team (triage, ticket resolution, coordination with Senior Manager…
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