Quality Control Analyst - Sao Paulo, Brasil - Johnson & Johnson

Johnson & Johnson

Empresa verificada

Sao Paulo, Brasil

há 2 semanas

Postado por:

Ana Silva

beBee Recruiter

Descrição

At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.

Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.

Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.

When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.

At Janssen, we're creating a future where disease is a thing of the past.

We're the Pharmaceutical Companies of Johnson & Johnson, working tirelessly to make that future a reality for patients everywhere by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart.

We focus on areas of medicine where we can make the biggest difference:
Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Hypertension.

We are Janssen.

Our mission drives us.

Our patients inspire us.

We collaborate with the world for the health of everyone in it.

We are searching the best talent for Quality Control Analyst ( 10 MONTHS
) to be in Sao Jose dos Campos.

Purpose:

The QUALITY CONTROL ANALYST will cooperate with quality control activities associated to company's project, ensuring internalization and deployment of quality requirements to the diverse processes of our supply chain.

You will be responsible for:

Perform activities related to the validation of analytical methodologies for drug products and raw materials / process validation / analytical tests in general (chemical activities)
Perform activities related to the validation of analytical methodologies for drug products and raw materials
Development, review, and execution of analytical validation protocols
Development and review of technical documentation and analytical validation reports
Support other activities/projects related to the analytical area
Structure and manage quality records

Eg:
investigations, CAPAs, and risk assessments

Ensure compliance with applicable regulations, standards and procedures
Ensure compliance with Data Integrity
Elaborate and Review documents at TRU according to methods transfers (protocol and reports)
Perform the transfer timeline of execution
Support other analysts of the project
Perform deep dive in the methods to support equipment team
Elaboration and review of technical documentation. (PATE, HMP, Technical Justification, Change Control Assessment and Risk Documentation)
Update/ obsolete documents, procedures, and specifications
Ability to communicate clearly with internal organization and global teams
Collaborate effectively with project members, following priorities, checkpoints, and deadlines to support objectives
Have the mindset to proactively find opportunities to improve our process.

Qualifications:

Qualifications:

University degree in pharmacy, chemistry, chemistry engineer, or related areas.
Minimum 2 years of work experience in quality control laboratory or analytical development.
Knowledge of physicochemical analyses: liquid and gas chromatography (HPLC ad CG), UV/IR spectroscopy, dissolution techniques, and others.
Good organization skill with ability to meet deadlines
Intermediate English (speak, written and listening)
Knowledge of the main pharmaceutical legislation (RDC 166/2017, RDC 73/2016, RDC 443/2020, RDC 53/2015, RDC 318/2019).
Quality processes and tools knowledge nonconformance, change control and laboratory investigations.
Empower and eLIMS experience.