Director, Aseptic Dp Process Engineering

Johnson & Johnson

Wilson, North Carolina, United States of America
Not specified; not specified; not specified
Fully onsite (with frequent travel over 75% until project shifts to plant site in wilson, nc)
15+ years drug product experience
Cgmp aseptic manufacturing expertise
Process engineering leadership
Johnson & Johnson is seeking a Director of Aseptic Drug Product Process Engineering to lead technical aspects of process engineering for a new aseptic manufacturing facility in Wilson, North Carolina. The role requires extensive experience in drug product development, strong leadership skills, and a commitment to compliance with industry standards

Job Summary

  • The role serves as the technical expert providing end-to-end process engineering leadership for the design and startup of a new aseptic manufacturing node.
  • Candidates must possess deep knowledge of cGMP regulations including FDA and EU standards, specifically the impact of new EU Annex 1 guidelines on facility design.
  • This position requires leading high-performing multicultural teams and managing complex capital projects ranging from $100 to $500 million.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Director of Aseptic Drug Product Process Engineering to lead technical aspects of process engineering for a new aseptic manufacturing facility in Wilson, North Carolina. The role requires extensive experience in drug product development, strong leadership skills, and a commitment to compliance with industry standards.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • 15+ years drug product experience
  • cGMP aseptic manufacturing expertise
  • Process engineering leadership
  • Capital project execution 100-500MM$
  • Commissioning and Qualification principles
  • EU Annex 1 regulatory fluency

Nice-to-have

  • Inclusive leadership culture
  • Data-driven decision making
  • Mentoring engineering talent
  • Multicultural team management
  • Strategic industry benchmarking

Key Requirements

  • Bachelor's degree in Engineering (Mechanical or Chemical)
  • Minimum 15 years biotherapeutics cGMP experience
  • Minimum 5 years people leadership experience
  • Experience with Commissioning & Qualification (C&Q)
  • Strong understanding of EHS by design

Work Rights

Not specified

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