Manager, Regulatory Affairs
hace 5 meses
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 are searching the best talent for** a Regulatory Affairs Manager **to be in **Bogota, Colombia **.**
**Purpose**:The Regulatory Affairs Manager is responsible for the overall management of the Regulatory Affairs activities to support and grow and the maintenance of the business in line with the company goals. The Manager leads all the regulatory affairs activities in LA North Cluster for the therapeutic areas under her/his responsibility.
**Essential Duties**:
- Obtain and maintain marketing authorizations - define and implement the registration strategy for new products and maintenance of products on the market.
- Ensure fast introduction of new products and line extensions, including new indications.
- Maintain and support communications with Health Authorities and third parties.
- Ensure regulatory compliance.
- Streamline regulatory activities with other business partners.
**Qualifications**:
**Qualifications**
- University Degree Completed.
- Advanced English level
- Skills Ability to learn and effectively convey clinical and non-clinical technical information; fast Learner; ability to network and matrix, ability to work independently, ability to lead and influence key decision makers, ability to develop and maintain strong relationships
- Minimum of 2 years of previous academic experience or industry related.
- Leadership and influence.
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