Principal Process Engineer– Device Assembly (da)

Johnson & Johnson Johnson & Johnson · Pharma · Wilson, NC +1

Principal Process Engineer for Device Assembly (DA) at Johnson & Johnson, focusing on end-to-end process engineering ownership of device assembly equipment for large-molecule, aseptic biotherapeutic drug product operations. Responsibilities include leading design, commissioning, qualification, and start-up activities, ensuring compliance with cGMP and regulatory requirements.

What you'd actually do

  1. Leads development and delivery of device assembly specifications and drawings (user requirements, data sheets, technical specifications, P&IDs, PFDs) supporting large-molecule, aseptic biotherapeutic drug product operations
  2. Provide process system ownership and technical leadership for aseptic device assembly equipment used in biotherapeutic drug product manufacturing
  3. Assess vendor competency and capabilities, review and influence bid documents, and maintain accountability for project development and execution, including system performance
  4. Lead detailed design and development of aseptic device assembly equipment, collaborating with multi-functional partners and strategic equipment vendors
  5. Serve as the Device Assembly equipment SME for large-molecule, aseptic drug product projects, collaborating with A&E firms, construction partners, and equipment suppliers

Skills

Required

  • Bachelor's Degree in engineering (Mechanical Engineering preferred)
  • 7 years device assembly equipment process engineering and/or device assembly capital project execution experience within a large-molecule, biotherapeutic cGMP environment
  • Strong background in aseptic, large-molecule, biotherapeutic drug product device assembly principles
  • Experience leading device assembly process engineering activities across the full product lifecycle, preferably within capital project execution
  • Ability to build and maintain positive relationships with multi-functional partners
  • Demonstrated strength in resolving complex technical and regulatory challenges impacting the equipment and facility design of device assembly equipment for large-molecule, biotherapeutic products
  • Solid understanding of cGMP requirements for aseptic device assembly equipment
  • Solid understanding of EHS requirements, with emphasis on EHS-by-design and construction safety
  • Solid understanding of Start-up processes and Commissioning & Qualification (C&Q) of aseptic equipment
  • Solid understanding of Engineering design principles for biotherapeutic drug product manufacturing
  • Solid understanding of Construction, procurement, project controls, and project scheduling
  • Strong technical depth, problem-solving capability, interpersonal skills, and decision-making ability in a fast-paced environment

Nice to have

  • MS or MBA preferred
  • Demonstrated leadership of capital projects for aseptic large-molecule, biotherapeutic device assembly equipment in the $50-$100 MM range
  • Deep process engineering expertise from conceptual design through C&Q to operational readiness in large-molecule biotherapeutic drug product environments
  • Experience supporting greenfield or brownfield GMP aseptic manufacturing facility start-ups in device assembly equipment

What the JD emphasized

  • cGMP
  • aseptic device assembly equipment
  • large-molecule, biotherapeutic drug product