Sr. Process Engineer

Johnson & Johnson Johnson & Johnson · Pharma · Jacksonville, FL +1

This role is for a Sr. Process Engineer in the contact lens supply chain organization, focusing on technical leadership for complex engineering projects. Responsibilities include process characterization, change control, validation/qualification (IQ/OQ/PQ), technical investigations, continuous improvement, and cross-functional delivery within a regulated GMP/ISO/FDA environment. The role requires a Bachelor's degree in a relevant engineering field and at least 4 years of experience in a regulated manufacturing setting.

What you'd actually do

  1. Leads and delivers complex engineering and/or change control projects requiring concept evaluation, design, and validation.
  2. Plans and delivers qualification of new or modified equipment, controls, systems, processes, and/or packaging operations; supports vendor and site acceptance testing (FAT/SAT) as required.
  3. Identifies and implements process, equipment, packaging, and/or materials enhancements that improve efficiency, yield, reliability, robustness, and safety.
  4. Leads structured problem solving and root cause analysis for complex quality, technical, and manufacturing issues (e.g., deviations, nonconformances, audit actions, CAPAs).
  5. Provides mentoring and technical guidance to junior engineers, interns, and/or co-ops; builds capability within the team.

Skills

Required

  • Bachelor's degree in Chemical Engineering, Materials Science Engineering, or related technical subject area
  • 4 years of relevant engineering experience in a manufacturing, operations, R&D, or similar regulated industry environment
  • Demonstrated experience leading projects of moderate-to-high complexity (multi-functional scope, qualification/validation, change control)
  • Strong analytical and structured problem solving capability
  • Ability to interpret data, identify trends, and drive decisions using risk-based thinking
  • Proven technical writing capability

What the JD emphasized

  • regulated (GMP/ISO/FDA) environment
  • validation/qualification activities (IQ/OQ/PQ)
  • technical investigations
  • continuous improvement
  • cross-functional delivery
  • complex engineering projects
  • process characterization
  • change control
  • structured problem solving
  • root cause analysis