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Quality Assurance Project Coordinator

3 meses atrás

São José dos Campos, São Paulo, Brasil Kenvue Tempo inteiro

Position Overview

Kenvue is seeking a dedicated professional for the role of Quality Assurance Project Coordinator. This position is integral to our Quality structure and will be based at our manufacturing site.

About Kenvue

At Kenvue, we harness the remarkable potential of everyday care. With a legacy spanning over a century and a foundation in scientific innovation, we proudly represent iconic brands such as NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON'S, and BAND-AID. Our global team, comprising 22,000 diverse and talented individuals, is driven by insights and innovation, committed to delivering exceptional products to our customers. We prioritize people, foster trust through science, and tackle challenges with courage, creating brilliant opportunities for our team members.

Key Responsibilities

The Quality Assurance Project Coordinator will oversee project management within the Quality Strategic Office, reporting directly to the Regional Quality Performance Manager. This role is pivotal in executing quality initiatives across the manufacturing site, ensuring compliance and excellence in various processes, including:

  • Quality Assurance
  • Quality Control
  • Research & Development Analytical
  • Manufacturing
  • Engineering

Specific duties include:

  • Leading quality initiatives related to the separation program.
  • Fostering collaboration across diverse functional areas with business partners.
  • Aligning with project sponsors and coordinating with core and extended teams to achieve project objectives.
  • Developing, managing, and maintaining comprehensive project plans in collaboration with cross-functional team members.
  • Ensuring effective coordination across all workstreams to meet project deliverables while adhering to quality standards.
  • Conducting project governance activities, including resource, risk, and scope management.
  • Managing change control processes to ensure compliance with quality and regulatory requirements.
  • Proactively identifying and addressing potential risks and issues.
  • Preparing and communicating project status updates regarding milestones, deliverables, and risks.
  • Serving as the PMO Point of Contact for functional teams, representing Quality and acting as a Subject Matter Expert for PMO tools.

Qualifications

Required Qualifications:

  • Bachelor's degree in pharmacy, chemical engineering, or a related technical field.
  • A minimum of seven years of relevant experience in a regulated health industry environment.
  • Experience with quality systems, audits, inspections, and regulatory compliance.
  • Proven ability to lead teams in dynamic, cross-functional settings.
  • Project management certification is preferred.
  • Strong technical knowledge in quality and regulatory matters.
  • Familiarity with LATAM GxP regulations applicable to cosmetics, devices, and pharmaceuticals.

Desired Qualifications:

  • Ability to inspire and motivate teams.
  • Exceptional problem-solving and conflict resolution skills.
  • Proven track record of effective cross-functional collaboration.
  • Flexibility and adaptability in a multifaceted environment.
  • Attention to detail and commitment to data accuracy and integrity.
  • Strong collaboration, urgency, analytical, and influencing skills.
  • Understanding of project controls and scheduling.
  • Ability to build and maintain relationships and partnerships.
  • Proficiency in English and Spanish.

What We Offer

We provide a competitive benefits package, including:

  • Paid company holidays and vacation time.
  • Opportunities for learning and development.
  • Access to employee resource groups.

Join us in our mission to shape the future of care and make a meaningful impact on the lives of millions.