Processing Operator I

Processing Operator I

Lo que hacemos

En Kenvue, nos damos cuenta del extraordinario poder del cuidado diario. Sobre la base de más de un siglo de herencia y arraigados en la ciencia, somos el hogar de marcas icónicas, incluidas NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® y BAND-AID® que ya conoces y amas. La ciencia es nuestra pasión; El cuidado es nuestro talento.

Quiénes somos

Nuestro equipo global está formado por ~ 22.000 personas brillantes con una cultura laboral en la que cada voz importa y cada contribución es apreciada. Nos apasionan las ideas, innovación y comprometidos con la entrega de los mejores productos a nuestros clientes. Con experiencia y empatía, ser un Kenvuer significa tener el poder de impactar a millones de personas todos los días. Ponemos a las personas en primer lugar, nos preocupamos ferozmente, nos ganamos la confianza de la ciencia y resolvemos con coraje, ¡y tenemos oportunidades brillantes esperándote! Únase a nosotros para dar forma a nuestro futuro y al suyo. Para obtener más información, haga clic en aquí.

Role reports to:

Senior Processing Supervisor

Ubicación:

North America, Canada, Ontario, Guelph

Lugar de trabajo:

Totalmente in situ

What will you

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.

Si usted es una persona con una discapacidad, consulte nuestra página de Disability Assistance para obtener información sobre cómo solicitar una adaptación.