Quality Control Analyst
1 semana atrás
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).
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