Sr. Princ. Process Engineer – Dp Aseptic Biotherapeutic Device Assembly And Packaging Equipment

J&J FAMILY OF COMPANIES

Wilson, North Carolina, United States
Fully remote
Aseptic device assembly and packaging
Large-molecule biotherapeutic drug product
Capital project execution experience
Johnson & Johnson is seeking a Senior Principal Process Engineer to lead the end-to-end process engineering for device assembly and packaging equipment in aseptic biotherapeutic drug product operations. The role requires strong technical expertise and collaborative leadership skills within a fast-paced, innovative healthcare environment

Job Summary

  • As part of the Global Process Engineering team, the Sr. Princ. Process Engineer serves as the recognized technical authority and Subject Matter Expert for device assembly and packaging equipment.
  • This role is accountable for end‑to‑end process engineering ownership from conceptual design through commissioning, qualification, and commercial manufacturing start-up.
  • Johnson & Johnson provides an inclusive work environment respecting diversity and merit, committed to equal opportunity employment and accommodating applicants with disabilities.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Principal Process Engineer to lead the end-to-end process engineering for device assembly and packaging equipment in aseptic biotherapeutic drug product operations. The role requires strong technical expertise and collaborative leadership skills within a fast-paced, innovative healthcare environment.

Skills & Requirements

Must-have

  • Aseptic device assembly and packaging
  • Large-molecule biotherapeutic drug product
  • Capital project execution experience
  • Process engineering lifecycle leadership
  • Cross-functional stakeholder partnership
  • Commissioning and qualification (C&Q)
  • Serialization and aggregation implementation

Nice-to-have

  • Leadership of capital projects $50–$100MM
  • Greenfield and brownfield facility start-ups
  • Combination products regulatory knowledge
  • Multicultural team leadership
  • Data-driven technical decision making
  • Innovation in aseptic equipment design
  • Strong problem-solving and communication

Key Requirements

  • Bachelor’s degree in Engineering
  • Minimum 10 years device assembly and packaging process engineering
  • Experience in large-molecule biotherapeutic cGMP environment
  • Strong aseptic drug product device assembly knowledge
  • Experience with commissioning and qualification (C&Q)
  • Ability to travel frequently (>75%)
  • Preferred Master’s degree or MBA

Work Rights

Not specified

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