Processing Operator 1

Kenvue; Guelph; On-site; CAD 36,000 - 58,000; Full time

Benefits offered by this job

Competitive Benefit Package

Paid Company Holidays

Volunteer Time & More!

Learning & Development Opportunities

Kenvuer Impact Networks

Job summary

Kenvue in Guelph, Ontario, is hiring a Processing Operator I to support the manufacturing of bulk pharmaceutical products. You will document activities in a regulated environment, working with Weigh & Dispense, Granulation, Compression, Finishing, and Liquids, under supervision.

The role requires GMP awareness, mechanical aptitude, and experience in a regulated facility. On-site, with competitive benefits and growth opportunities at Kenvue.

Qualifications

• Grade 12 education and GMP compliance understanding.
• Mechanical aptitude with GMP environment experience.
• Proficiency in MS Word, Excel, and SAP.
• Post-secondary education in chemistry/biochemistry/biology preferred.
• 2-3 years in a regulated pharma/manufacturing environment.
• Experience in solid dose manufacturing in OTC/pharma facility.
• Previous mechanical experience or training.

Responsibilities

• Successfully execute all manufacturing steps for cleaning, setup and operations in the assigned work center.
• Process raw materials per validated processes and SOPs; follow batch/ cleaning records.
• Monitor and record processing parameters with accurate documentation.
• Perform SAP/MES transactions and ensure data recording in Plant Cockpit system.
• Maintain updated training records and adhere to timelines.
• Identify safety issues and complete safety training.
• Identify quality concerns and report deviations per GMP/GDP.

Skills

Mechanical aptitude

GMP understanding

Education

Grade 12 Education

Post-secondary in chemistry/biochemistry/biology

Tools

MS Word

Excel

SAP

Job description

Processing Operator 1

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.

Role reports to

Processing Supervisor

Location

North America, Canada, Ontario, Guelph

Work Location

フルオンサイト

What you will do

Description

Under minimal direction, the ProcessingOperator Iperforms 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.

Key Responsibilities

• Successfully execute all manufacturing steps associated with cleaning/sanitation, set-up and manufacturing operations associated with the assigned work center.
• Process raw materials according to validated processes and SOPs. Follow all instructions in batch and cleaning records.
• Monitor and record processing parameters and maintain accurate documentation.
• Perform appropriate SAP/MES transactions, ensuring timely and complete data recording in the Plant Cockpit system.
• Maintain updated training records and adhere to training timelines.
• Ensure a safe working environment by identifying potential safety issues and completing all required safety training.
• Ensure quality and compliance by identifying potential quality concerns, adhering to GMPs and GDPs, and reporting deviations.

What we are looking for

Required Qualifications

• Grade 12 Education
• Understanding of GMP compliance
• Mechanical aptitude
• Proficiency in MS Word, Excel, and SAP

Desired Qualifications

• Completion of post-secondary education in a relevant field (e.g., chemistry, biology, biochemistry)
• 2-3 years of experience in a regulated (food or pharmaceutical) manufacturing environment
• Experience in solid dose manufacturing in an OTC or pharmaceutical facility
• Previous mechanical experience or training

What’s in it for you

Annual base salary for new hires in this position ranges:$36,000.00 - $57,730.00

• 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 screeningofapplications, 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.