Quality Control Analyst

Há 4 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.

**Quality Control Analyst (Fixed Term - 12 months) JANSSEN SJC**

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.

**Key Responsibilities**:

- 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**

**Education**:

- 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.

**Experience and Skills**

**Required**:

- 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.

**Preferred**:

- 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.

**Other**:

- Language: Advanced English (speak, written and listening).
- No travel is required for this position.

**Primary Location**
Brazil-São Paulo-São José dos Campos-Rod.Presidente Dutra, Km 154

**Organization**
Janssen Cilag Farmaceutica Ltda. (7585)

**Job Function**
Quality

**Requisition ID**
2206075054W

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