Who We AreAt 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. Ourglobal team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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.PROPÓSITO FUNDAMENTAL Y ALCANCE:The MBR configurator will perform the following functions:* Communicating with MBR designers, production and lab process creators and CSV and Data Integrity experts to configure the required Master Batch Report (MBR).* He/she is responsible for delivering the MBRs following the designed processes and complying with the data integrity and compliance guidelines indicated for them by the experts in charge, in a timely manner.* He/she will be responsible for the maintenance and modification of these MBRs once they are in use based on the procedures in force and the requirements of the plants and projects assigned to him/her.* Participate in the execution of development, commissioning and validation tests as support or executor as required in each case according to the procedures in force and the project structure.MINIMUM QUALIFICATIONS:* Required Education: A bachelor's degree in computer science, Information Systems,* Engineering, Chemical, Pharmacy or another related field required; relevant experience maybe substituted when appropriate; additional certifications a plus.* Required Experience: A minimum of 2 years of progressive industry experience with direct experience in Manufacturing, Laboratory and/or Quality in GxP (Regulated Environment Good Practices) environments. Experience authoring, approving or reviewing manufacturing and lab SOP, Work Instruction, Batch Record and Laborator Notebooks and Logbooks deliverables, Non-conformities, Investigations and Reports.* Required Skills: Knowledge of Data Integrity, GDP, cGMP regulations related to Manufacturing, Lab and Product Release. Quality and manufacturing error-proof process design oriented.
