Biotherapeutics MSAT Fellow: Emerging Technologies

Biopharma Careers; North Carolina; On-site; USD 164,000 - 279,000; Full time

Job summary

Johnson & Johnson is seeking a Fellow in Emerging Technologies, MSAT, to define solutions for advanced manufacturing and Real Time Release. You will mentor teams, pursue external collaborations, and help shape the roadmap for process intensification across laboratory and pilot scales.

The role requires a PhD with 10–12 years of experience in chemical/biochemical engineering or related fields, with strong QA, QbD, and cGMP familiarity. Domestic/international travel up to 20% is expected.

Qualifications

• Minimum requirements: BA/BS, PhD with minimum 10-12 years of experience
• Education in a technical field related to pharmaceutical manufacturing is preferred.

Responsibilities

• High-impact contributor shaping advanced manufacturing solutions.
• Scout and benchmark new technologies for biotherapeutic drug substance manufacturing.
• Identify relationships within internal and external partners (academic, government, commercial).
• Provide technical mentorship to Emerging Technologies organization and ensure solutions are tested and adopted.
• Oversee lab and pilot-scale studies to develop new technologies and innovations.

Skills

Biochemical Engineering

Chemical Engineering

Process Optimization

Quality Assurance (QA)

SAP Product Lifecycle Management

STEM Application

Research and Development

Critical Thinking

Commercial Awareness

Consulting

Design Mindset

Disruptive Innovations

Performance Measurement

Process Chemistry

Education

BA/BS and PhD in a related field

Technical field related to pharmaceutical manufacturing (e.g., Chemical Engineering, Bioengineering, Biomedical Engineering, Chemistry)

Tools

SAP Product Lifecycle Management

Job description

Johnson & Johnson is seeking a Fellow in Emerging Technologies, MSAT, to define solutions for advanced manufacturing and Real Time Release. You will mentor teams, pursue external collaborations, and help shape the roadmap for process intensification across laboratory and pilot scales.

The role requires a PhD with 10–12 years of experience in chemical/biochemical engineering or related fields, with strong QA, QbD, and cGMP familiarity. Domestic/international travel up to 20% is expected.