CAR-T Document Specialist Technical Writer

Company: Disability Solutions
Location: Raritan
Posted on: September 29, 2024

Job Description:

Johnson & Johnson is recruiting for a CAR-T Warehouse Document Specialist/Technical Writer! This onsite position is in Raritan, New Jersey!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 MedTech, 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 https://www.jnj.com/.For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR T platform and investigational treatment.Are you interested in joining a diverse team delivering outstanding results to our customers? Apply now for this exciting opportunity!The CAR -T Warehouse Document Specialist/Technical Writer will primarily build, update, and maintain technical documents and communications related to warehouse processes, as needed. Their writing will adhere to set standards regarding order, clarity, conciseness, style, and terminology. Special projects may require this individual to gather and prioritize data from various departments and implement this research into their own work.Key Responsibilities:

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• Continuous improvement of all GMP documents to ensure they are streamlined and robust, easy to use, and intuitive
• Ensure quick turnaround time of document updates to prevent disruption in operations
• Stay current on industry standards and ensure that all GMP documents incorporate the latest regulatory and quality requirements
• Supervise the revision process of existing SOPs in-time to support manufacturing strategies
• Ensure that accurate training is prescribed as per document changes made
• Assure regulatory compliance and technical feasibility of proposed document changes
• Serves as Subject Matter Expert (SME) in preparation for and during internal and external regulatory audits (including FDA, EMEA)\r\r

Keywords: Disability Solutions, Plainfield , CAR-T Document Specialist Technical Writer, Advertising , Raritan, New Jersey