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. Business Unit Manager, ProcessingLocation:
North America, Canada, Ontario, GuelphWork Location:
Fully OnsiteWhat you will do
The Process Engineer supports continuous improvement within the Processing area by leading and executing projects that improve safety, quality, efficiency, and cost effectiveness. Following an initial training period supporting the Senior Process Engineer, the incumbent transitions to independently managing projects and technical activities.
The role also supports deviation investigations, corrective action identification and implementation, effectiveness checks, and equipment qualification and validation. Working cross-functionally with internal stakeholders and external partners, the Process Engineer applies statistical and problem-solving tools to validate improvements and leads projects to completion on time and within budget.
Key Responsibilities
Plan, schedule, and execute engineering projects that evaluate, select, adapt, or modify manufacturing techniques, procedures, and criteria to improve Processing operations.
Provide technical direction and support for continuous improvement initiatives, including the implementation of technologies that improve safety, quality, efficiency, or cost performance.
Monitor equipment and process performance, conduct root cause problem solving for key downtime drivers, and develop effective action plans to improve operational performance.
Support equipment qualification and validation activities, including FAT, SAT, DQ, IQ, OQ, and PQ, as directed.
Lead or participate in investigations related to nonconformances, complaints, audit observations, and Corrective and Preventive Actions, including trend analysis and communication.
Partner with Operators, Maintenance, Quality, Technical Operations, and Processing stakeholders to identify and implement equipment repairs, equipment improvements, and process changes.
Support equipment acquisition activities, including user requirement specifications, equipment selection, installation, validation, employee training, and related documentation.
Prepare protocols, reports, presentations, training documents, standard operating procedures, and other technical documentation for internal and external stakeholders.
What We Are Looking For
Required qualifications :
Bachelor of Engineering degree.
Minimum of 2 years of related engineering experience.
Demonstrated ability to work effectively in a team-based and cross-functional environment.
Strong problem-solving skills, with the ability to investigate issues and identify underlying causes.
Excellent written and verbal communication skills.
Self-directed, with the ability to manage competing priorities and meet deadlines.
Strong interpersonal skills and the ability to communicate effectively with internal stakeholders, vendors, and contractors.
Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint.
Desired qualifications :
Bachelor’s degree in Chemical Engineering, Mechanical Engineering, or a related engineering discipline.
Experience in solid-dose manufacturing or packaging within an over-the-counter or pharmaceutical facility.
Experience with tablet manufacturing for consumer goods or pharmaceutical products.
Understanding of Good Manufacturing Practice quality systems.
Knowledge of Lean Manufacturing principles and experience applying them in an operational environment.
What’s in it for you
Annual base salary for new hires in this position ranges:$61,000.00 - $97,175.00
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*
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.
Kenvue incorporates Artificial Intelligence into our recruitment process to enhance job postings and streamline the sorting and screening of applications, helping attract a qualified candidate pool. Our experienced team will review and select the top applicants, ensuring that human judgment guides our hiring decisions. For more information, please refer to our Careers Privacy Policy.
Vacancy: This job posting is for an existing, currently vacant position.
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