Senior Cell Processing Engineer – Duration-based Role

Job not on LinkedIn

🔥 2 hours ago

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $122k - $212.8k / year

⏰ Full Time

🟠 Senior

🧑‍💻 Full-stack Engineer

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Johnson & Johnson

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

🧘 Wellness

Pharmaceuticals • Biotechnology • Wellness

<Johnson & Johnson> is a global healthcare company that researches, develops, manufactures and markets pharmaceuticals, medical devices and consumer health products. The company focuses on innovative medicines and therapies across oncology, immunology, neuroscience and cardiopulmonary areas, and develops MedTech solutions in cardiovascular, orthopaedics, surgery and vision. Johnson & Johnson also engages in health & wellness education, large-scale manufacturing, investor activities and global social-impact initiatives.

📋 Description

• Lead site master planning by translating capacity, technology, compliance, and business needs into facility and operational plans aligned with site strategy. • Provide technical leadership for Grade A equipment planning, installation, commissioning, qualification, and readiness, including isolators and aseptic processing technologies. • Lead CAR-T automation projects from assessment and business case input through implementation, testing, governance, and adoption. • Develop user requirements, support testing, assess process fit, and drive readiness for new equipment, automation platforms, systems, and processes. • Prioritize opportunities to improve efficiency, automation, reliability, cost, compliance, and risk reduction, with clear path-forward recommendations. • Direct operational documentation, including procedures, work instructions, electronic batch records, training materials, and change management outputs. • Represent Operations in key decisions across facility planning, equipment and process design, qualification, validation, technology transfer, and automation. • Apply aseptic processing, contamination control, closed processing, biosafety, and advanced therapy manufacturing expertise. • Apply technical and operational judgment to resolve complex issues and support scalable, compliant, inspection-ready operations.

🎯 Requirements

• Minimum of 8 years of relevant work experience. • Experience in cGMP manufacturing, facility design, site master planning, aseptic equipment installation, isolator technology, automation implementation, technology transfer, validation, or quality operations. • Demonstrated ability to collaborate across internal and external partners in a matrixed environment. • Ability to work independently, manage multiple priorities, lead through change, and translate cross-functional issues into practical solutions. • Strong communication skills with ability to influence peers, provide direction, and support decision making.

🏖️ Benefits

• Vacation –120 hours per calendar year • Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year • Holiday pay, including Floating Holidays –13 days per calendar year • Work, Personal and Family Time - up to 40 hours per calendar year • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child • Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year • Caregiver Leave – 80 hours in a 52-week rolling period • Volunteer Leave – 32 hours per calendar year • Military Spouse Time-Off – 80 hours per calendar year