Analista de Qualidade Pleno - 2406197180W

Description

Johnson & Johnson is currently seeking an Analista de Qualidade Pleno to join out team located in Sao Jose dos Campos

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong

Purpose:

The JnJ PL Quality Analyst will be able to manage all quality system activities.

You will be responsible for:

• Management of quality topics as: change control, documentation and training, supplier qualification, licenses, controlled substances, pest control, environmental monitoring and batch release.

• Control and monitor Quality KPIs

• Knowledge in change control management process (mandatory).

• Gap assessment of policies and legislations to assure local procedures complies with GxP rules.

Qualifications

Qualifications :

• University/bachelor’s degree in pharmacy, chemistry engineering, or related science fields.

• Minimum of 2-5 years of work experience in quality systems.

• Teamwork

• Good communication, with the ability to communicate with different levels of the organization.

• Focus on quality continuous improvement.

• Knowledge of the main pharmaceutical legislation (RDC 658/2022, RDC 430/2022, and others relevant to GxP).

• Ability to communicate in English (speak, written and listening).

Primary Location Latin America-Brazil-São Paulo-São José dos Campos

Organization Janssen Cilag Farmaceutica Ltda. (7585)

Job Function Quality Assurance

Req ID: 2406197180W