Principal Engineer

Kenvue is currently recruiting for a:Principal EngineerWhat we doAt 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 AreOur 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 doThe 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 ResponsibilitiesEngineering Project LeadershipLead engineering projects across all phases (concept, planning, design, implementation, qualification, and stabilization)Develop project scope, user requirements, capital requests, budgets, schedules, and risk mitigation plansManage procurement, installation, startup, commissioning, and qualification of equipment and systemsEnsure projects are delivered on time, within budget, and in full compliance with regulatory and corporate standardsTechnical Expertise & Operational SupportServe as technical subject matter expert for manufacturing equipment, processes, and systemsProvide troubleshooting support and lead quality investigations and root-cause analysesDrive process optimization and continuous improvement initiatives across productivity, quality, safety, and costIntroduce innovative designs, technologies, and engineering solutions aligned with business strategyCompliance, Quality & EHSEnsure full adherence to cGMPs, Good Documentation Practices, and FDA-regulated expectationsReview and approve Change Controls, Commissioning & Qualification plans, protocols, and reportsChampion Environmental, Health & Safety standards, ISO 14001 principles, and site sustainability initiativesPromote a strong culture of safety, compliance, and "right-first-time" executionLeadership & CollaborationLead cross-functional and external project teams, including contractors and consultantsMentor and provide technical guidance to engineers and project teamsBuild strong partnerships with Quality, Operations, Supply Chain, Validation, and Regulatory teamsPresent project proposals, updates, and recommendations to site and senior leadershipStrategic & Financial AccountabilityOwn project capital plans, cashflow forecasts, scope management, and long-range engineering strategiesContribute to 5-year asset replacement planning, automation, and reliability roadmapsMonitor industry trends, benchmarks, and emerging technologies to inform future investmentsQualificationsEducationBachelor's degree in Engineering (Chemical, Mechanical, Electrical, or related discipline required)Advanced degree preferredExperience8+ years of engineering experience in pharmaceutical, biotech, medical device, or consumer products manufacturingStrong background in capital project execution within an FDA / cGMP-regulated environmentProven experience with commissioning, qualification, and regulatory complianceSkills & CompetenciesDeep understanding of cGMPs, GDP, and quality systemsStrong project management, analytical, and problem-solving skillsAbility to lead complex initiatives under minimal supervisionEffective communication and stakeholder influence at all levelsProficiency with common engineering and business tools (MS Office, data analysis, validation documentation)Certifications (Preferred)Project Management certificationSix Sigma Green Belt or Black BeltWork EnvironmentPrimarily office and manufacturing floor environmentOccasional exposure to production areas, equipment, solvents, noise, and industrial materialsFlexibility to support off-hours activities during critical project phases or emergenciesWhat's in it for youAnnual base salary for new hires in this position ranges:$124,100.00 - $175,200.00This 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 OpportunitiesKenvuer Impact NetworksThis 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.

Created: 2026-04-02