Kenvue is currently recruiting for a Principal Engineer.
What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information, click here.
Role Reports to:
Sr Manager Engineering and Automation
Location: North America, United States, Pennsylvania, Lititz
Work Location: Fully Onsite
What you will do
The Principal Engineer provides technical leadership and engineering support to a regulated manufacturing environment. This role leads complex capital and process improvement projects from concept through post‑implementation, ensuring compliance with cGMP, safety, quality, cost, and timeline commitments. The incumbent acts as a recognized technical authority, partners cross‑functionally, and delivers engineering solutions that support productivity, quality, sustainability, and long‑term business objectives.
Key Responsibilities
Engineering Project Leadership
Lead engineering projects across all phases (concept, planning, design, implementation, qualification, and stabilization)
Develop project scope, user requirements, capital requests, budgets, schedules, and risk mitigation plans
Manage procurement, installation, startup, commissioning, and qualification of equipment and systems
Ensure projects are delivered on time, within budget, and in full compliance with regulatory and corporate standards
Technical Expertise & Operational Support
Serve as technical subject matter expert for manufacturing equipment, processes, and systems
Provide troubleshooting support and lead quality investigations and root‑cause analyses
Drive process optimization and continuous improvement initiatives across productivity, quality, safety, and cost
Introduce innovative designs, technologies, and engineering solutions aligned with business strategy
Compliance, Quality & EHSE
Ensure full adherence to cGMPs, Good Documentation Practices, and FDA‑regulated expectations
Review and approve Change Controls, Commissioning & Qualification plans, protocols, and reports
Champion Environmental, Health & Safety standards, ISO 14001 principles, and site sustainability initiatives
Promote a strong culture of safety, compliance, and "right‑first‑time" execution
Leadership & Collaboration
Lead cross‑functional and external project teams, including contractors and consultants
Mentor and provide technical guidance to engineers and project teams
Build strong partnerships with Quality, Operations, Supply Chain, Validation, and Regulatory teams
Present project proposals, updates, and recommendations to site and senior leadership
Strategic & Financial Accountability
Own project capital plans, cashflow forecasts, scope management, and long‑range engineering strategies
Contribute to 5‑year asset replacement planning, automation, and reliability roadmaps
Monitor industry trends, benchmarks, and emerging technologies to inform future investments
Qualifications
Education
Bachelor's degree in Engineering (Chemical, Mechanical, Electrical, or related discipline required)
Advanced degree preferred
Experience
8+ years of engineering experience in pharmaceutical, biotech, medical device, or consumer products manufacturing
Strong background in capital project execution within an FDA / cGMP‑regulated environment
Proven experience with commissioning, qualification, and regulatory compliance
Skills & Competencies
Deep understanding of cGMPs, GDP, and quality systems
Strong project management, analytical, and problem‑solving skills
Ability to lead complex initiatives under minimal supervision
Effective communication and stakeholder influence at all levels
Proficiency with common engineering and business tools (MS Office, data analysis, validation documentation)
Certifications (Preferred)
Project Management certification
Six Sigma Green Belt or Black Belt
Work Environment
Primarily office and manufacturing floor environment
Occasional exposure to production areas, equipment, solvents, noise, and industrial materials
Flexibility to support off‑hours activities during critical project phases or emergencies
What's in it for you
Annual base salary for new hires in this position ranges: $124,100.00 - $175,200.00
This takes into account a number of factors including work location, the candidate's skills, experience, education level & other job-related factors.
Competitive Benefit Package
Learning & Development Opportunities
Kenvuer Impact Networks
This list could vary based on location/region
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.