MBR Configurator - Madrid, España - Kenvue

Descripción

Who We Are

At [company], we understand the incredible power of everyday care. With a rich heritage of over a century and a foundation in science, we are the home to renowned brands like NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S, and BAND-AID that are already close to your heart. Science drives our passion, and care defines our expertise. Our global team consists of 22,000 vibrant and diverse individuals, all dedicated to bringing innovative insights and the best products to our customers. Being part of Kenvuer means having the ability to positively impact millions of lives every single day. Putting people first, caring deeply, earning trust through science, and solving challenges with courage are at the core of what we do - and there are fantastic opportunities awaiting you to join us in shaping our future, and yours. To learn more about us, please visit our website.

PROPÓSITO FUNDAMENTAL Y ALCANCE:

The MBR configurator will be responsible for:

• Collaborating with MBR designers, production and lab process creators, as well as CSV and Data Integrity experts, to configure the necessary Master Batch Reports (MBRs).
• Ensuring timely delivery of MBRs in accordance with established processes and compliance guidelines set by the responsible experts.
• Managing the maintenance and adjustments of MBRs post-implementation based on current procedures and the requirements of assigned plants and projects.
• Engaging in the execution of development, commissioning, and validation tests as either support or executor based on project needs and existing protocols.

MINIMUM QUALIFICATIONS:

• Education: Bachelor's degree in computer science, Information Systems, Engineering, Chemical, Pharmacy, or a related field; relevant experience can be considered, and additional certifications are a plus.
• Experience: At least 2 years of progressive industry experience with a focus on Manufacturing, Laboratory, and/or Quality in GxP environments. Hands-on experience with authoring, approving, or reviewing manufacturing and lab SOPs, Work Instructions, Batch Records, Laboratory Notebooks, Logbooks, Non-conformities, Investigations, and Reports.
• Skills: Proficiency in Data Integrity, GDP, cGMP regulations within Manufacturing, Lab, and Product Release. Strong orientation towards designing error-proof processes in Quality and manufacturing.

Primary Location

Europe/Middle East/Africa-Spain-Community of Madrid-Madrid

Job Function

Production