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Specialist, Quality Systems & ComplianceKenvue is currently recruiting for this position, reporting into the Quality structure based at Kenvue SJC, BRAZIL site, but the base location is Cali, Colombia.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 deliver quality plans across the region 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 ResponsibilitiesTake lead on quality projects related to the separation program (spin‐off).
Build collaboration across different functional areas with business partners.Build alignment with Sponsor, aligning Core and Extended teams 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.Open and manage change controls 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 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.QualificationsWhat we are looking for:Required QualificationsBachelor's degree in pharmacy, chemical engineering, or an equivalent technical field.A minimum of 7 years of relevant professional work experience in the regulated health industry, including cosmetic/device/drug regulations.Experience in quality systems, audits/inspections, and regulatory affairs.Proven experience leading virtual teams within dynamic regional/cross‐functional environments (ideally 3–5 years).
Project management certification is preferred.Solid technical knowledge of quality/regulatory requirements.Understanding of LATAM GxP regulations applicable to cosmetics, devices, and pharmaceuticals.Advanced English proficiency.Desired Qualifications / Technical CompetencesAbility to lead and motivate teams.Excellent problem‐solving and conflict resolution skills.Consistent track record of working cross‐functionally.Flexibility and adaptability to thrive in a multifaceted environment.Attention to detail and a drive for ensuring data accuracy and integrity.Strong collaboration, sense of urgency, analytical, and influencing skills.Understanding of project controls and scheduling.Ability to develop and maintain relationships/partnerships and work collaboratively.What's In It For YouCompetitive Benefit Package.Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More.Learning & Development Opportunities.Employee Resource Groups.This list may vary based on location/region.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, protected veteran status, or disability.Primary Location: Latin America – Colombia – Valle del Cauca – Cali.Job Function: Quality (Generalist).
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📌 Quality Supervisor (Fixed Term 12 Months) (Cali)
🏢 Kenvue
📍 Valle del Cauca