Processing Operator I

Processing Operator I

Cosa facciamo

A Kenvue, ci rendiamo conto dello straordinario potere della cura quotidiana. Costruiti su oltre un secolo di tradizione e radicati nella scienza, siamo la casa di marchi iconici, tra cui NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® e BAND-AID® che già conosci e ami. La scienza è la nostra passione; la cura è il nostro talento.

Chi siamo

Il nostro team globale è composto da ~ 22.000 persone brillanti con una cultura del posto di lavoro in cui ogni voce conta e ogni contributo è apprezzato. Siamo appassionati di intuizioni, innovazione e impegno a fornire i migliori prodotti ai nostri clienti. Con competenza ed empatia, essere un Kenvuer significa avere il potere di avere un impatto su milioni di persone ogni giorno. Mettiamo le persone al primo posto, ci prendiamo cura di noi, ci guadagniamo la fiducia della scienza e risolviamo con coraggio - e abbiamo brillanti opportunità che ti aspettano! Unisciti a noi per plasmare il nostro futuro e il tuo. Per ulteriori informazioni, fare clic su here.

Role riporta a:

Senior Processing Supervisor

Ubicazione:

North America, Canada, Ontario, Guelph

Luogo di lavoro:

Completamente in loco

Cosa farai

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.

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

• 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.

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