MSAT Emerging Technology & Labs DP Fellow

The person we are looking for serves as a technical expert, shaping and defining solutions for advanced manufacturing that support Process Intensification and Real Time Release, with a final aim of process reliability, enhancements, and control. They will also guide and mentor those around you, shaping our advanced manufacturing roadmap. Identify, pursue and maintain relationships with internal and external partners, academic, government, and commercial, using MSAT, MTO and DPDS resources as needed. Identify areas of the highest impact on implementation of new technologies, focusing on broad applicability and ease of introduction. Strong record of contributing to business through identification of internal and externa technologies, and the breakthrough application of these technologies to create competitive products and processes (new or improved processes or products, Trade Secrets, Patents/Publications) through discovery and/or Licensure., * High-impact individual contributor influencing and shaping the strategic direction of advanced manufacturing solutions that deliver high value competitive products and processes.

• You will scout and benchmark new technologies and advancement in biotherapeutic drug product manufacturing
• Identify, pursue, and maintain relationships within internal and external partners such as academic, government, and commercial.
• You will be a technical mentor, guide, and support the entire Emerging Technologies organization; working closely with leads to ensure the best solutions are tested and driven towards adoption.

• Minimum requirements: BA/BS, PhD with minimum 10-12 years of experience
• Education in a technical field related to pharmaceutical manufacturing, such as Chemical Engineering, Bioengineering, Biomedical Engineering, Chemistry, or a similar quantitative scientific field is preferred., * An outstanding track record of delivering meaningful solutions and strategic directions for next generation pharmaceutical manufacturing in both Biotherapeutics and Synthetics fields.
• Significant expertise in pharmaceutical manufacturing, with a focus on biotherapeutic or parenteral drug product processes and associated unit operations, including impacts to GxP regulations.
• Outstanding skills in scientific communication, including authoring documents (white papers, publications) and excellent visual display of quantitative information.

Preferred:

• Sound grasp of Quality by Design principles and Pharmaceutical Real time release testing.
• Familiarity with manufacturing cGMPs, Systems Qualification, Process Validations, process sciences, Tech Transfers, QbD, advanced analytical technology, PAT, Continuous Manufacturing, Modular Manufacturing.
• Familiarity with modeling (chemometric, mechanistic, machine learning, AI)
• A history of external influencing scientific fields through white papers, presentations, publications in relevant fields and a strong network in academia and industry.

Other:

• Proficient English, both written and spoken
• Requires up to 20% domestic and international travel.

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 jnj.com. 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.