Quality Control Analyst

Há 2 dias

Sao Paulo, Brasil Johnson & Johnson Tempo inteiro

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 (Fixed Term - 12 months) **to be in **São José dos Campos - SP **.

**Purpose**:The Janssen Quality Analyst will support overall activities associated to the analytical development laboratory team, driving activities related to the validation and transfer of analytical methodologies for drug products and raw materials.

**You will be responsible for**:

- Perform activities related to the validation and transfer of analytical methodologies for drug products and raw materials.
- Develop and review analytical protocols and reports.
- Develop and review technical documentations.
- Conduct investigation and evaluation of non-conforming results.
- Structure and manage quality records. E.g: investigations, CAPAs, change controls and, risk assessments.
- Act as a leader in project management of transfers and analytical validations.
- Support other activities/projects as required.

**Qualifications**:
**Qualifications and requirements**:

- University/bachelor’s degree in chemistry, pharmacy, engineering, or related areas.
- Desirable a minimum of 3 years of work experience in Analytical Laboratory in Pharmaceutical, Cosmetics, or Medical Device company.
- Proactive profile.
- Good organization skill with ability to meet deadlines.
- Ability to handle multiple tasks simultaneously.
- Analytical, prioritization, and good communication skills, with the ability to communicate with different levels of the organization.
- Strong team player with the ability to work across a diverse team.
- Knowledge of the main pharmaceutical legislation (RDC 166/2017, RDC 73/2016, RDC 443/2020, RDC 53/2015, RDC 318/2019 and others relevant to R&D).
- Knowledge of analytical techniques: liquid chromatography (HPLC), gas chromatography (GC), UV/IR spectroscopy, dissolution techniques, and others.
- Desirable 3 years of previous experience in transfer and validation of analytical methodologies, elaboration of technical documentations (PATEs and technical justifications) and physical chemical analyzes.
- Language: Advanced English (speak, written and listening).

  • Quality Control Analyst

    Há 7 dias

    São Paulo, Brasil TriMas Corporation Tempo inteiro

    **Quality Control Analyst** Company: Rieke do Brasil Embalagens Ltda. Primary Location: Avenida Juvenal Arantes, nº 2500, Galpão 19, Condo, Jundiai, Sao Paolo, 13212-15, BRA Employment Type: Salaried | Full-Time Function: Quality Equal Opportunity Employer Minorities/Women/Veterans/Disabled **Main Duties & Responsibilities** **Position Summary**:The...

  • Quality Control Analyst

    1 semana atrás

    São Paulo, Brasil Kaizen Gaming Tempo inteiro

    **We are Kaizen Gaming** Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 17 markets. We always aim to leverage cutting-edge technology, providing the best experience to our millions of customers who trust us for their entertainment. We are a diverse team of more than 2.700 Kaizeners, from 40+...

  • Quality Control Analyst

    2 semanas atrás

    São Paulo, São Paulo, Brasil Rieke do Brasil Embalagens Ltda. Tempo inteiro US$40.000 - US$80.000 por ano

    Quality Control AnalystCompany: Rieke do Brasil Embalagens Ltda.Primary Location: Avenida Juvenal Arantes, nº 2500, Galpão 19, Condo, Jundiai, Sao Paolo BRAEmployment Type: Salaried | Full-TimeFunction: QualityEqual Opportunity Employer Minorities/Women/Veterans/Disabled Main Duties & ResponsibilitiesPosition Summary:The Quality Analyst evaluates...

  • Quality Control Analyst

    4 semanas atrás

    São Paulo, São Paulo, Brasil Kaizen Gaming Tempo inteiro

    **We are Kaizen Gaming**Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 17 markets.We always aim to leverage cutting-edge technology, providing the best experience to our millions of customers who trust us for their entertainment.We are a diverse team of more than 2.700 Kaizeners, from 40+...

  • Quality Assurance Analyst

    2 semanas atrás

    Sao Paulo, Brasil Novo Nordisk Tempo inteiro

    Quality Assurance Analyst **Category**:Quality**Location**:São Paulo, São Paulo, BR- **The Position** - As a Quality Assurance Analyst at Novo Nordisk, you will play a pivotal role with the following key responsibilities: - Operationalize the Quality Management System (QMS) and uphold Good Warehousing and Distribution Practices (GWDP) with Sanitary...

  • Quality Control Analyst

    3 semanas atrás

    São Paulo, São Paulo, Brasil Johnson & Johnson Tempo inteiro

    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...

  • Quality Assurance Analyst Jr

    2 semanas atrás

    Sao Paulo, Brasil Novo Nordisk Tempo inteiro

    Quality Assurance Analyst Jr **Category**:Quality**Location**:São Paulo, São Paulo, BR- **The Position** - As a Quality Assurance Analyst Jr. at Novo Nordisk, you will take on the following key responsibilities: - Operationalize the Quality Management System (QMS) and uphold Good Warehousing and Distribution Practices (GWDP) with Sanitary Technical...

  • Quality Assurance Analyst

    2 semanas atrás

    São Paulo, São Paulo, Brasil beBeeQualityAssurance Tempo inteiro R$74.526 - R$127.438

    Job OverviewWe are seeking a highly skilled Quality Assurance Analyst to join our team. As a key member of our quality assurance team, you will be responsible for ensuring the highest standards of product quality and manufacturing operations.The ideal candidate will have a strong background in pharmacy and extensive experience in quality assurance. You will...

  • Quality Control Analyst

    1 semana atrás

    Sao Paulo, Brasil Johnson & Johnson Tempo inteiro

    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...

  • Quality Assurance Analyst

    2 semanas atrás

    São Paulo, São Paulo, Brasil Novartis Brasil Tempo inteiro

    Overview Quality Assurance Analyst role at Novartis Brasil. Responsibilities Oversight of all production and testing activities, ensuring compliance with cGxP, data integrity, and eCompliance within the Novartis Quality Management System. Support exception investigations; review and approval of production, QC, and AS&T records; MBR review. Support OpEx...