Jobs in Canada

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Technician (Full Time)
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Added 14 mins ago
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Operator Technician I - Fixed Term 12 months | Second Shift
Kenvue
Guelph, ON
- Full-time
This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
Added 14 mins ago
K
Processing Operator 1 - Night shift - Fixed term 12months
Kenvue
Guelph, ON
- Full-time
Processing Operator 1 - Night shift - Fixed term 12months · Processing Night Shift Supervisor

Kenvue

Processing Operator 1 - Night shift - Fixed term 12months

Guelph, ON, Canada

Full-time

Apply on kenvue.wd5.myworkdayjobs.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 30, 2026
Experience: 2-3 years of experience in a regulated (Food or Pharmaceutical) Manufacturing environment
Posting language: English
Posted: Nov 13, 2026

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.

What we are looking for:

Required qualifications:

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:

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 on kenvue.wd5.myworkdayjobs.com About employer

More about this job

Responsibilities

The Processing Operator performs manufacturing tasks for bulk pharmaceutical products, including weighing, dispensing, granulation, and compression. They are responsible for maintaining accurate documentation, monitoring processing parameters, and ensuring compliance with GMP and SOP standards.

Requirements

Candidates must have a minimum of a Grade 12 education, mechanical aptitude, and proficiency in MS Word, Excel, and SAP. Previous experience in a regulated manufacturing environment, particularly in solid dose manufacturing, is highly desired.

Skills

Manufacturing
GMP Compliance
Mechanical Aptitude
SAP
MS Word
Excel
Pharmaceutical Processing
Troubleshooting
Data Recording
Sanitation
Batch Record Documentation
Solid Dose Manufacturing
Problem-solving
Quality Control

Benefits

Paid Company Holidays
Paid Vacation
Volunteer Time
Learning & Development Opportunities
Competitive Benefit Package

Visa sponsorship

Not detected in the job text

Keywords

Manufacturing
Pharmaceutical
GMP
SOP
SAP
MES
Processing Operator
Bulk Pharmaceutical Products
Weigh & Dispense
Granulation
Compression
Coating
Printing
Mechanical Aptitude
Plant Cockpit
Downtime Tracking
Solid Dose Manufacturing
OTC
Quality Assurance
Documentation

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Work requirements

Jobs in Canada