About this role
Kenvue is currently recruiting for a: Process Improvement Engineering Intern 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: Cosmetic Filling Manager Location: Europe/Middle East/Africa, Italy, Lazio, Rome Work Location: Fully Onsite What you will do Kenvue is currently recruiting: Process Improvement Engineering Intern This position reports into Cosmetic Filling Manager and is based in Pomezia Santa Palomba (Rome). Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment 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.
La ricerca è aperta a candidati di entrambi i sessi e rivolta anche a persone appartenenti alle categorie protette (L. 68/99) . Valutiamo con favore candidature che contribuiscano alla diversità e all’inclusione.
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®, 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 .
What will you do Support in the following activities: Ensures GMP, EHS and Quality requirements are met in the area of responsibility. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. To approve the instructions relating to production operations and to ensure their strict implementation.
To ensure that the production records are evaluated and signed by an authorized person before they are sent to the Quality Assurance Department. To check the maintenance of the departments, premises and equipment. To ensure that the appropriate validations are done.
To ensure that the required initial and continuing training of the department personnel is carried out and adapted to the need. Actively drives and encourages the identification and implementation of continuous improvements initiatives within the Production. Key Responsibilities: Quality and Compliance: Ensures compliance of production related activities with all relevant quality, compliance legislation, SOP’s, Master Instructions and Kenvue policies as delegated by the Responsible Pharmacist.
Therefore, there is a pharmaceutical reporting line to the Responsible Pharmacist. Ensures that relevant SOP’s, manufacturing procedures and packing documentation are prepared and reviewed Ensures GMP by maintaining production area and equipment in a clean and good working order; maintaining tidiness and minimising cross contamination risks Manages & over-sees manufacturing operations & ensures batches are manufactured according to registered methods Participates in management reviews as per GMP requirements EHS: Ensures product is manufactured to the required EHS standards and guidelines Implements EHS SOPs and MAPs Ensures that staff fully complies to PPE requirements in the production area Monitors waste generation and implement waste reduction action plans Production planning and scheduling Schedules agreed production plan in conjunction with planners to optimise manufacturing operations to achieve maximum utilization of resources Ensures capacity is available, including people, equipment and materials in order to execute the required production plan Ensures necessary communication forums are in place for personnel, e.g. morning feedback meetings. Liaises with support functions to facilitate the production plan Production/Operations: Executes production activities in accordance with agreed production plan.
Optimizes utilization of manufacturing resources to achieve cost efficient usage of labour, capacity and materials Drives performance to ensure that Production targets are met Initiates trouble-shooting, problem solving and resolution of any obstacles in achieving agreed supply plan Ensures that company scorecard goals and objectives are achieved Ensures continuous improvement to reduce costs, increase productivity and improve quality Encourages staff participation in process improvement projects Maintenance: Ensures plant and equipment are managed and maintained to achieve optimal performance Ensures that preventative maintenance work is carried out in accordance with schedules Ensures that validation activities are carried out as required Ensures all change over’s done as per the required work standard Human Resources: Manages and motivates staff to achieve the agreed production plan Ensures all staff is trained in accordance with the identified training plans What we are looking for Required Qualifications Master’s Degree in Mechanical or Management Engineering. Desired Qualifications Knowledge in Lean manufacturing. Knowledge of Lean/ SixSigma / 5S methodology is highly recommended; Upper-intermediate in English; Proven knowledge in MSOffice package.
Personal Attitudes Has good leadership and team building attitudes supported by technical skills. With a structured mindset can analyze data and drive problem solving with a strong attitude to change and improve the status quo with a proper deployment and reapplication. Enables the organization to grow consistently ensuring proper deployment, training and standard mindset.
With a Continuous improvement and Zero Waste mindset, has a lateral thinking, challenging status quo in never-ending research for optimization. Has scarcity mentality with pragmatic less-for-more approach. Seeks for the root cause and with a continuous learning and improving approach and is aiming to look for solution to fix to the root cause focusing forward.
Complement motivation and engagement with analytical databased method. What’s in it for you Competitive Benefit Package Learning & Development Opportunities Employee Resource Groups Monthly reimbursement of 800 euros If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.