Regulatory Affairs Jr Analyst

**Regulatory affairs jr analyst**:
At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for 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 Next Move Could Mean Our Next Breakthrough

At Johnson & Johnson Medical Devices Companies, we are using our breath, scale and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.

In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.

We are hiring the best talent for REGULATORY AFFAIRS JR ANALYST

to be located in BUENOS AIRES (Relocation Not Applicable / Applicable).

**Purpose**:
The objective of this position is to have an ally who is eager to learn and to be inserted in the Medical Devices Industry. For this, you will be provided with many tools that will allow you to develop and learn more every day.

In this role, you will be carrying out regulatory affairs activities needed to follow the requirements of Local Heath Authority. You will gather, prepare and upload regulatory documentation for registrations of medical devices.

You will use regulatory documentation management systems, you will interact with many stakeholders throughout LATAM and participate in projects that are of your interest.

**Key Responsibilities**:

- Ensures compliance with regulatory agency regulations and interpretations.
- Prepares responses to regulatory agencies' questions and other correspondence.
- Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines. Develops timelines for submissions.
- Manage the company's systems for different activities related to the position.
- Skills for teamwork, good communication and organization are highly appreciated.

**Qualifications**
**Qualifications and Requirements**:
**Education**:
An advanced student or degree in Health Sciences is needed, preferably Pharmacist, Biochemist or related.

**Skills**:
Upper Intermediate or Advance level of English.

Systems management skills.

Well-organized with attention to detail.

A high degree of initiative and curiosity.

**Primary Location**
Argentina-Buenos Aires-Villa Adelina
- **Organization**
Johnson & Johnson Medical S.A. (7435)
**Job Function**
Regulatory Affairs
**Requisition ID**
2206024390W