Logo
Johnson & Johnson Innovative Medicine

Senior Principal Cell Processing Robotics Engineer

Johnson & Johnson Innovative Medicine, Titusville, New Jersey, us, 08560

Save Job

Senior Principal Cell Processing Robotics Engineer

Johnson & Johnson Innovative Medicine is recruiting for a Senior Principal CAR-T Robotics Engineer. This hybrid position can be based in Titusville, NJ; Spring House, PA; or Raritan, NJ. Job Function:

Supply Chain Engineering Job Sub Function:

Automation Engineering Job Category:

Scientific/Technology Job Description

We apply science-driven approaches to develop the medicines of tomorrow. This role focuses on cell processing mechatronics and robotics within the CAR-T program, driving ownership across design, qualification, startup, and transition to operations. You will collaborate with R&D, Operations, MSAT, Quality, and external partners to enable automated, GMP-compliant cell processing solutions in a next-generation manufacturing setting. The CAR-T Engineering organization oversees the asset portfolio and related business processes for JJIM’s Advanced Therapies Supply Chain. The Senior Principal CAR-T Robotics Engineer is a technical owner of cell processing mechatronics systems, supporting design credibility, vendor relationships, and successful system turnover to end users. Responsibilities include ensuring flawless execution during project design, qualification, startup, and transition; leading safety reviews and ensuring compliance with applicable standards; developing asset management procedures; driving continuous technical improvements; and supporting problem solving as needed. Role also involves developing knowledge of CAR-T manufacturing processes and aseptic/cell processing techniques, and partnering with multiple functions to optimize automation and manufacturing deliverables. Key Responsibilities

Represent Engineering in Facility & Equipment Design, Qualification and Startup, through transfer to the end user; support tech transfer through process validation and regulatory approval. Write or support User Requirement Specifications (URSs), Change Controls, Impact Assessments, and other technical documents; ensure business requirements are incorporated into the design. Own Mechatronics/Robotics equipment and technology; build relationships with equipment partners and provide cross-functional technical support. Ensure robotics deliverables meet project timelines and budget. Coordinate third-party engineering and design services, including RFPs and objective bid analysis. Engage with vendors for FAT/SAT within the system of responsibility with E&PS lead. Participate as Mechatronics/Robotics SME; own safety reviews (EHS by Design, HAZOPs, machine safety, ergonomics). Ensure compliance with safety standards (ANSI/RIA R15.06, ISO 10218-1, ISO 13849, and other regulations). Develop an integrated process data map and criticality assessments for automation and manufacturing deliverables. Own cost and resources within the system of responsibility; develop asset management procedures, PM, maintenance and calibration. Drive standards for the asset portfolio and provide asset ownership as a service for production/lab equipment and utilities. Support asset lifecycle activities, including replacement planning and vendor evaluation/selection. Support investigations, deviations, CAPAs, and timely compliance closures; participate in inspections/audits. Ensure compliance with cGMPs, EU Annex 1, global regulatory requirements, safety, environmental regulations, SOPs, and corporate standards. Communicate regularly with the Engineering community and share CAR-T expertise globally. Analyze processes to identify optimization opportunities, efficiency improvements, and cost savings. Additional Focus – CAR-T Production Knowledge Develop in-depth understanding of CAR-T manufacturing processes and aseptic/cell processing techniques. Build robust understanding of cell processing robotics and automation; stay current with GMP and ATMP regulatory frameworks. Qualifications

Education: Bachelor’s Degree in Mechanical or Electrical Engineering required; Mechatronics/Advanced Manufacturing/Automated Systems preferred. Experience and Skills (Required): Minimum 8 years of relevant work experience. Experience in Manufacturing Operations and/or Engineering; familiarity with process automation and robotics. CAD proficiency; understanding of robotics and automation. Programming: C++, Python, and/or MATLAB. Control systems, signal processing, and PLCs familiarity. Experience with commissioning/qualification/validation of equipment and systems; IT manufacturing systems. Pharma/Biopharma/Large Molecule or cell therapy experience is an asset; hands-on asset ownership experience. Vendor management, change control, and asset replacement experience. In-depth knowledge of GMP standards and related guidelines (ISO, EN, ICH, FDA, ISPE). Ability to prioritize, manage changing deadlines, and collaborate across teams. Service mindset with hands-on engineering and asset ownership experience. Strong collaboration in a matrix environment; startup mindset and solution orientation. Ability to work independently and manage multiple tasks; strong cross-functional integration. Preferred: Experience with Staubli robotics, Robot Operating Systems (ROS), AI, and IoT. Other Requires up to 50% travel (domestic and/or international). The anticipated base pay range is $120,000 to $207,000. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other protected characteristics. Accommodation requests for applicants with disabilities can be directed via the company careers page. Employment Type:

Full-time Job Function:

Engineering and Information Technology Industries:

Pharmaceutical Manufacturing

#J-18808-Ljbffr