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Kenvue

Processing Operator 1 - Night shift - Fixed term 12months

Guelph, ON, Canada

Pay: Annual base salary for new hires in this position ranges:$41.000,00 - $66.470,00
Job type: Full-time
Apply by: Oct 28, 2026
Experience: 2-3 years of experience in a regulated (Food or Pharmaceutical) Manufacturing environment
Posting language: English
Posted: Sep 28, 2026

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Original job description

Kenvue Is Currently Recruiting For a

Processing Operator 1 - Night shift - Fixed term 12months

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

Processing Night Shift Supervisor

Location:

North America, Canada, Ontario, Guelph

Work Location:

Fully Onsite

What You Will Do

Under minimal direction, the Processing Operator I performs all responsibilities necessary associated with the manufacturing of bulk pharmaceutical products and the accurate documentation of these activities in a regulated manufacturing environment.

The core manufacturing functions include Weigh & Dispense, Granulation, Compression, Finishing (Coating & Printing) and Liquids

This is to work on Night Shift and is a 12 month Fixed term contract

Key Responsibilities

Successfully execute all manufacturing steps associated with cleaning/sanitation, set-up and manufacturing operations associated with the work center the operator has been assigned to.
Processes raw materials according to the validated process identified on the batch record, cleaning record, and SOPs, and follows all steps/instructions in batch records, cleaning records, and SOPs.
Monitor and record all processing parameters and maintain all necessary processing and cleaning/sanitation documentation.
Performs appropriate SAP/MES transactions in accordance with the SOP. Ensures accurate, timely and complete data recording of progress and downtime events in the Plant Cockpit system. Department goal of 95% completion of downtime events.
Maintains an updated and current training record and adheres to training timelines.
A Compression Operator will face challenges in understanding tablet compression, troubleshooting defects such as weight variation, capping, and sticking, and balancing critical machine settings like compression force, fill depth, and press speed to maintain product quality. They must also develop strong mechanical and problem-solving skills, learn how different formulations behave, follow GMP and documentation requirements accurately, and stay focused during long production runs to identify issues before they impact quality or efficiency. The most successful operators learn not just how to run the press, but how to understand and control the compression process.

Required Qualifications

What we are looking for:

Minimum of a Grade 12 Education
Understanding of GMP compliance is required
Mechanical aptitude is essential
Proficiency in MS Word, Excel and SAP is required.

Desired Qualifications

Completion of a post-secondary education
2-3 years of experience in a regulated (Food or Pharmaceutical) Manufacturing environment
Preferred experience in solid dose manufacturing in an OTC or Pharmaceutical Facility.
Previous mechanical experience or training would be an asset.

What’s In It For You

Annual base salary for new hires in this position ranges:$41.000,00 - $66.470,00

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.

Apply About employer

More about this job

Responsibilities

Perform cleaning, sanitation, equipment setup, and manufacturing operations for bulk pharmaceutical products, following validated processes, batch records, cleaning records, and standard operating procedures. Monitor and document processing parameters, complete SAP/MES and downtime transactions, and maintain current training records in a regulated manufacturing environment.

Requirements

A Grade 12 education, understanding of GMP compliance, mechanical aptitude, and proficiency in Microsoft Word, Excel, and SAP are required. Post-secondary education and 2–3 years of regulated food or pharmaceutical manufacturing experience are desired; solid-dose manufacturing and mechanical experience are preferred assets.

Skills

GMP Compliance
Mechanical Aptitude
Manufacturing Operations
Cleaning and Sanitation
Equipment Setup
Raw Material Processing
Batch Record Documentation
Standard Operating Procedures
Process Monitoring
Data Recording
SAP
MES
Microsoft Word
Microsoft Excel
Tablet Compression
Troubleshooting

Benefits

Competitive Benefits Package
Paid Company Holidays
Paid Vacation
Volunteer Time
Learning and Development Opportunities

Visa sponsorship

Not detected in the job text

Keywords

Good Manufacturing Practices
Regulated Manufacturing
Pharmaceutical Manufacturing
Bulk Pharmaceutical Products
Solid-Dose Manufacturing
Over-The-Counter Products
Weighing and Dispensing
Granulation
Tablet Compression
Finishing
Coating
Printing
Liquids Processing
Cleaning and Sanitation
Equipment Setup
Batch Records
Cleaning Records
Standard Operating Procedures
Process Parameters
SAP
Manufacturing Execution System
Plant Cockpit
Downtime Tracking
Mechanical Aptitude
Troubleshooting
Microsoft Word
Microsoft Excel

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