About this role
Kenvue is currently recruiting for a:
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 AutomationLocation:
North America, United States, Pennsylvania, LititzWork Location:
Fully OnsiteWhat 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 & EHS
- 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:
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
Paid Company Holidays, Paid Vacation, Volunteer Time & More!
Learning & Development Opportunities
Kenvuer Impact Networks
This list could vary based on location/region
Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.
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.
Other facts
About Kenvue
Kenvue is the world’s largest pure-play consumer health company by revenue. Built on more than a century of heritage and propelled forward by science, our iconic brands — including Aveeno®, BAND-AID® Brand Adhesive Bandages, Johnson’s®, Listerine®, Neutrogena®, Tylenol® and Zyrtec® — are recommended by health care professionals and can be trusted by consumers who use our products to improve their daily lives. Our team members share a digital-first mindset, with an approach to innovation grounded in deep human insights and work every day to earn a place for our products in consumers’ hearts and homes. At Kenvue, we believe everyday care can not only make people well; it can make them whole.
Beware of recruitment scams: https://www.kenvue.com/media/recruitment-scams-alert
What you'll do
- The Principal Engineer provides technical leadership and engineering support to a regulated manufacturing environment, leading complex capital and process improvement projects. This role ensures compliance with cGMP, safety, quality, cost, and timeline commitments while delivering engineering solutions that support productivity and long-term business objectives.
Ready to join Kenvue?
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