.At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, **YOU **are welcome in all open positions at the largest healthcare company in the world.When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.Our vision is to be the best-in-class Health & Wellness organization by leveraging the commercial strategy to deliver competitive advantage and value creation for the consumer, customer, and J&J. And as part of one of the largest and most diverse healthcare companies in the world, our brands leverage the company's world-class research tools and scientific prowess to provide consumers across the globe with innovative consumer medicines, skin, baby, and essential health solutions.You deserve to work in a place where you feel well and welcome.We are searching the best talent for **QUALITY AND COMPLIANCE LABELING SUPERVISOR** to be in **Mexico City**.**Purpose**:The overall objective of this role is to support the labeling process and assist in maintaining the quality system and GxP compliance of ongoing quality operations at J&J LATAM organization. This position will report to Israel Meza - LAN Commercial Quality Head and dotted line to LATAM Q&C Project Diamond Leader (Renata Silva).**You will be responsible for**:- Perform all aspects of Quality assurance on labeling process; since labels set up, review and implementation in all J&J products that will face a change due to project DIAMOND execution, ensuring compliance to the applicable regulations (COFEPRIS, PROFECO, INVIMA, SIC, DIGEMID, Etc.) and J&J procedures / standards.- Serve as a GxP label inspector/auditor.- Review and Follow-up on labeling findings and ensure timeliness of closure.- Draft and revise reports as required.- Actively participate in the preparation, execution, and follow-up for labeling process.- Ensure that labels meet established requirements of cGMPs, J&J SOPs and enterprise policies.- Write and complete analysis of investigation (s), identify issues and provide recommendations for improvements.- Support assigned Quality projects - Tasks- Support internal / external audits when necessary**Calificaciones** Qualifications and requirements**:- Bachelor's Degree in Pharmacy / Chemistry / Biosciences / Engineering or equivalent, with 3 to 5 years industry experience in quality, labeling or cGMP, pharmaceutical/medical device quality systems- Inglés (escrito y hablado), Portugues (deseable)- 3 a 5 años de experiência en puesto afín