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Sr Eng Process Engineering

Job in Wilson, Wilson County, North Carolina, 27893, USA
Listing for: NCBiotech
Full Time position
Listed on 2026-08-05
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Validation Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 90000 - 150000 USD Yearly USD 90000.00 150000.00 YEAR
Job Description & How to Apply Below

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Wilson, North Carolina, United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at

Learn more and apply to this exciting new role!

Johnson and Johnson is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients. The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience. J&J’s significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations.

Learn more at

The Manufacturing Science and Technology (MSAT) department manages the process technology platform strategy to produce biotherapeutics in the new Bio Processing Facility in Wilson, North Carolina. We are responsible for Process, Thermal & Cleaning Validation, Standardization of Equipment for New Product Introduction, Process Analytics Introduction, and Life Cycle Management (LCM) of our commercial production processes.

We have a great opportunity for an MSAT Tech Transfer Engineer to join our MSAT LCM & Process Analytics team located in Wilson, NC!

Key Responsibilities
  • Active engagement with the MSAT team, delivering a successful outcome to MSAT Tech transfer activities for the Downstream process and Process Analytics implementation using Good Manufacturing Practices (GMP).
  • Primary activities are in the Tech transfer of new/commercial products as well as implementation of new technologies and/or digital tools for the Downstream process. Planning, documenting, and performing process validation studies.
  • Coordinate and execute MSAT Downstream process lifecycle management activities for new equipment, processes, and site startup initiatives in compliance with US and EU regulations and company procedures.
  • Coordinate and execute process improvement projects, commercial product scale-up initiatives, and technical transfer activities ensuring a successful implementation.
  • Apply technical expertise to offer second-line support to our Manufacturing Operations team as well as provide technical guidance for process improvement projects and investigations.
  • Track and resolve exceptions/events/nonconformances during MSAT activities.
  • Coordinate and prioritize MSAT activities in alignment with the applicable manufacturing and project schedules.
  • Implement, qualify, and maintain PAT tools (e.g., Raman spectroscopy, capacitance probes, soft sensors) to enable real‑time monitoring of upstream and downstream CQAs and CPPs.
  • Integrate PAT instrumentation with manufacturing data systems to support process control, process robustness, and continuous verification as well as analyze process data to identify trends, deviations, and sources of variability across biologics manufacturing operations.
  • Conduct statistical modeling, multivariate analysis (e.g. PCA/PLS), and batch trajectory analytics to support investigations, CPV, continuous improvement initiatives and detect early signals of process drift.
  • Support model lifecycle activities including development, validation, documentation, and ongoing performance monitoring in a GMP environment.
  • Able to author basic modeling-related documents (e.g., model development reports, analysis summaries).
  • Prepare, review, and approve technical documents, CAPAs, change control requests, investigations, protocols, reports, and SOPs, as needed.
  • Compile relevant information from contractors, suppliers, and other departments to develop technical reports.
  • Attend identified training required to fulfill the role of a Tech…
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