Come work at the forefront of science - and help the brands you grew up with grow and evolve into the next generation. Job Description - QUALITY SUPERVISOR (Fixed Term 12 months) (2407024967W) Specialist, Quality Systems & Compliance This position reports into Quality structure based at Kenvue SJC, BRAZIL site, but is based in Cali, Colombia. Who we are At Kenvue, part of the Johnson & Johnson Family of Companies, we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S and BAND-AID —are category leaders trusted by millions of consumers who use our products to improve their daily lives. What will you do The Project Quality Specialist will be responsible for Project management in the Quality Strategic Office organization, reporting to Regional Quality Project Manager. This role will be responsible for delivering quality plans across the region in order to achieve project separation milestones in several workstreams such as regulatory licensing, inspection readiness, quality management system adequacy, product label & codes change management, documentation updates including change control coordination and others. Key Responsibilities Take lead on quality projects related to separation program (spin off). Build collaboration across different functional areas with business partners. Build alignment with Sponsor, aligns Core and Extended team to deliver the Final Project Objectives. Develop, manage, and maintain up-to-date Project plans through collaboration with cross functional team members. Ensure seamless coordination across all workstreams, fostering cross-functional collaboration to maintain synchronization and meet project deliverables following quality requirements. Provide project governance activities across all workstreams such as resource management, risk management and scope management. Change control opening and management to track all GxP related activities on-time and in compliance with Kenvue procedures and country-specific quality/regulatory requirements. Manage risks effectively, identify potential problems early, and assist in resolving or raising issues as appropriate. Effectively prepare and communicate project status updates regarding project milestones, deliverables, and risks within the workstreams and for the broader project. Support the functional teams as a PMO Point of Contact as Quality representative and act as the SME for the PMO tools. Qualifications What We Are Looking For Required Qualifications Bachelor's degree in pharmacy, chemical engineering or equivalent technical field required. A minimum of 7 (seven) years of relevant professional work experience in the field regulated health industry: Cosmetic/Device/Drug regulations environment. Experience in Quality systems, audits/inspections and regulatory affairs. Proven experience in leading virtual teams within dynamic settings in a regional/cross-functional environment. Ideally 3-5 years. Project management certification is preferred. Solid technical (quality/regulatory) knowledge. Understanding of LATAM GxP regulations applicable for cosmetics, devices, pharmaceutical industries. Advanced English. Desired Qualifications /Technical competences Ability to lead and motivate teams. Excellent problem-solving and conflict resolution skills. Consistent track record to work cross-functionally. Flexibility and adaptability to thrive in a multifaceted environment. Attention to detail and a drive for ensuring data accuracy and integrity. Strong demonstrated collaboration, sense of urgency, analytical, influencing skills. Understanding of project controls and scheduling. Must be able to develop and maintain relationships/partnerships and to work collaboratively. What's In It For You Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More! Learning & Development Opportunities. Employee Resource Groups. 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. #J-18808-Ljbffr
