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Sr. Princ. Process Engineer – DP Aseptic Biotherapeutic Automated Optical Inspection Equipment

Job in Wilson, Wilson County, North Carolina, 27893, USA
Listing for: Johnson & Johnson
Full Time position
Listed on 2026-05-20
Job specializations:
  • Engineering
    Validation Engineer, Process Engineer, Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Job Function

Supply Chain Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

Location

Wilson, North Carolina, United States of America

Job Description

As part of the Global Process Engineering team, the Sr. Princ. Process Engineer serves as the recognized technical authority and Subject Matter Expert for manual and automated inspection equipment. This role is accountable for the end‑to‑end (E2E) process engineering ownership of manual and automated inspection equipment, from conceptual design, commissioning and qualification, and initial equipment start‑up for commercial manufacturing.

This role will be responsible for demonstrating their scientific, technical, and business expertise to develop the process/equipment, solve sophisticated equipment issues, optimize the process, lead commissioning and qualification activities and line start‑up and ensure compliance to regulatory standards.

Key Responsibilities
  • Act as the senior technical leader and Optical Inspection (OI) equipment owner, providing direction and oversight to internal teams and external partners (A&E firms, construction contractors, system integrators, and equipment vendors) to define scope, set expectations, and execute project strategies.
  • Demonstrated deep background and hands‑on expertise in optical inspection technologies, processes, and equipment within a cGMP, aseptic, large‑molecule biotherapeutic drug product environment.
  • Proven track record in leading the design, development, and implementation of manual and automated optical inspection processes and equipment, including recipe development and test kit design, supporting large‑molecule, biotherapeutic aseptic drug products.
  • Strong capability to develop and deliver automated inspection equipment specifications and engineering documentation, including User Requirements Specifications (URS), data sheets, technical specifications, P&IDs, and PFDs, aligned with aseptic processing and sterile manufacturing requirements.
  • Accountable for vendor evaluation and selection, including assessing vendor capabilities, reviewing bid packages, and ensuring performance expectations are met through project.
  • Demonstrated leadership in factory and site acceptance testing (FAT/SAT), commissioning, qualification (C&Q), and start‑up, ensuring systems are inspection‑ready and compliant with regulatory requirements.
  • Ability to resolve complex technical issues during design, installation, and C&Q phases, applying strong problem‑solving skills and sound engineering judgment on OI equipment.
  • Experience leading cross‑functional collaboration with Manufacturing, MSAT, Quality, Facilities, E&PS, Procurement, EHS, and external partners, acting as the primary technical authority for the OI equipment.
  • Solid understanding of EHS‑by‑design principles, construction safety requirements, and project execution processes in cGMP environments.
  • Ability to apply data‑driven insights, industry benchmarking, and technology trends to influence design decisions and continuously improve inspection system performance.
  • Demonstrated leadership skills to mentor, influence, and guide diverse and multicultural teams, ensuring technical knowledge is maintained and expanded across the organization.
Qualifications Education
  • Minimum of a Bachelor's Degree in engineering required (Mechanical Engineering preferred), MS or MBA preferred.
Required Experience and Skills
  • Minimum of 10 years optical inspection process engineering and/or capital project execution experience within a large‑molecule biotherapeutic cGMP environment.
  • Strong background in aseptic, large‑molecule, biotherapeutic drug product optical inspection principles.
  • Experience leading optical inspection process engineering activities across the full project lifecycle, preferably within a capital project execution environment.
  • Proven track record of developing and sustaining strong partnerships with key stakeholders, serving as a trusted technical authority across Engineering, Manufacturing, MSAT, Quality, Facilities, E&PS, Procurement, EHS, and project leadership.
  • Demonstrated ability to lead, influence, and motivate multicultural and geographically dispersed…
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