Quality and Compliance Make Excellence Sr Analyst - Sao Paulo, Brasil - Kenvue

Kenvue

Empresa verificada

Sao Paulo, Brasil

há 2 semanas

Postado por:

Ana Silva

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Descrição

Quality and Compliance Make Excellence Sr Analyst | São José dos Campos W

Description

Kenvue is currently recruiting for Quality and Compliance Make Excellence Sr Analyst and is based at São José dos Campos.

Who We Are

At Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), 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.

Our employees share a digital-first mindset, an approach to innovation grounded in deep human insights, and a commitment to continually earning a place for our products in consumers' hearts and homes.

Join us in shaping our future-and yours.

Watch us her

e:

What will you do

The Quality and Compliance Excellence Sr Analyst has the responsibility to actively support and work on the development, maintenance & continuous improvement of our Local Quality Management processes focusing on the internal manufacturing of São José dos Campos, whilst ensuring compliance, enabling consistency across the regional network, and leveraging global expertise.

The position will act as the expert, as an extension of the Regional Quality Excellence center within Internal Make in Supply Chain.

The position is responsible for ensuring the execution of the defined strategies and the leadership of implementation tactics for key projects; leading the development and implementation of procedures and protocols throughout quality engineering and process excellence tools to guarantee quality processes and standards are continuously evolving to achieve or exceeds business quality targets.

Partner with Make Excellence and other process improvement functions constantly looking to collaborate with operations, laboratory, engineering, and maintenance, to evaluate, develop and implement improvement projects to maintain or improve products and processes quality and robustness.

Among the main responsibilities, the individual will work with all areas to keep the financial governances in place, assuring financial results are achieved by the organization.

Additionally, must champions the needs of partners managing projects and initiatives to develop and introduce new processes & improve existing ones closely aligned with the regional quality and supply chain strategy,

Responsibilities

Act as the local expert for the excellence topics, who must constantly pursuit the development, maintenance & continuous improvement of our Quality Management processes
Manages project and initiatives, leading across functional teams to achieve desired results in an effective and timely manner.
Using statistical tool build analysis and provide insights from quality data that allows management to make strategic decisions, i

e:
creation of an executive summary; use of PE tools and concepts to analyze/drive process improvements as appropriate

Lead projects to develop and introduce new processes & improve existing processes, conduct needed analysis and develop appropriate learning activities across operational functions. Ensures adequate controls and cross functional resources are provided to meet projects requirements and schedule commitments.
Elevate Quality capabilities for SJC site (systems, process, and people) working closely with all Quality Excellence members within Latin America to drive standardization & simplification and ensure collaboration with the Regional & Global Quality teams.
Demonstrated ability to lead crossfunctional teams and collaborate with internal/external partners to enhance relationships and interactions
Proven ability to lead and influence others within product teams with excellent communication and presentation skills.
Detailoriented, with the ability to work in a fastpaced environment with multiple, concurrent priorities many needing immediate resolution.
This position may require up to 25% domestic and/or international travel.

Qualifications

Required Qualifications

A minimum of a Bachelor's degree or higher and at least 5 years in Quality Assurance is required.
Detailed working knowledge of cGMP requirements and is required.
Strong communication (verbal & written) and interpersonal skills, selfawareness and adaptability is required.
Experience and demonstrated skills in navigating in a matrix environment, managing complexity, collaborating across boundaries and influencing without authority is required.
Fluency in English / Advanced communication skills in Portuguese and Spanish is required

Desired Qualifications

GMP experience in Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production is preferred.
Master's Degree or higher is preferred.
Process Excellence I Six Sigma Certification o