Regulatory Affairs Coordinator Health Care

Job description

Description

Are you passionate about making sure every detail has been met?

All our roles provide competitive wages as well as the opportunity to engage and grow in your profession across growing categories. At this job, you will help deliver our brands advance to market and will support procedures to ensure the compliance of all product and retail packages.

Are you ready to be an awesome Regulatory Affairs Coordinator?

1.Perform regulatory activities for healthcare products.

2.Including medicines (Rx/OTC), working with projects.

3.New submissions and maintenance of marketing authorizations for Ecuador

4.Prepare and submit variations and renewals of our current portfolio.

5.Perform an adequate follow up of Health authority submissions.

6.Evaluate artworks and marketing promotional materials.

7.Providing adequate regulatory insight to the multifunctional team

8.Perform the necessary regulatory tasks to the registration process for P&G Health products.

9.Review and compile technical dossiers, ensuring that high quality data.

10.Track of submission and approvals, co-ordinate the preparation and conduct the review of responses to questions raised by the regulatory authorities.

11.Provide regulatory support to project teams, stakeholders and customers, as required.

12. Possibility to move between Quito and Guayaquil

What we offer you:

·  Significant work from your first day in P&G and every single day learning.
·  Environment multifunctional teamwork and high level of interaction with managers and directors who will develop your skills
·  Competitive salary and a benefit package.
·  We love flexibility. You can arrange your work schedule based on your personal needs.

How much do you know about us?

We offer meaningful challenges day one and effective and constant training. Thus, we bring to bear the strengths of our employees and develop them to become phenomenal leaders. In addition, diversity is very important for us: we seek the most diverse talent so that we always know how to innovate to exceed the expectations of our 5 billion consumers in the world. Therefore, working with us is the best opportunity to do what you love, with constant challenges and to be recognized for its results. More than that, it's the ideal opportunity to help us touch and improve billions of lives in our world.

For over 175 years, we have built some of the world’s most successful brands, including Ariel®, Tide®, Pantene®, Pampers®, and Gillette®. We believe in serving the consumer and ensuring our organization, talent and brand building reflects the diversity and needs of the approximate 5 billion people around the world we serve through our brands. We value leadership as well as deep understanding and offer fulfilling career opportunities that make us an unbeatable force in our industry.

We are an equal opportunity employer and value diversity at our company.

·  You'll not be discriminated on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Qualifications

Qualifications required for this role:

·  Chemical Pharmacy science degree or Life Science Degree
·  Regulatory experience preferably in healthcare areas.
·  5 years experience in registration of products in Ecuador.
·  Must have experience of the pharmaceutical environment, and life cycle management
·  Intermediate to advanced English level
·  Skills: Good communication.
·  Able to work under pressure and to tight timelines.
·  Effective time and organization management
·  Teamwork/collaboration.
·  Results oriented
·  Entrepreneurial and self-motivating.
·  Commercial understanding of corporate and operational business issues.
·  Openness to change and ability to think out of the box.
Job locations:
Guayaquil, Provincia del Guayas, Ecuador; Quito, Provincia de Pichincha, Ecuador Job Type: Full-time Req No: RND00004426