Regulatory Affairs Intern

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Istanbul, Turkey

Job Description:

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

We are looking for Long Term Intern to join our Regulatory Affairs Team based in Istanbul, Turkey. If you are interested in Pharma regulatory activities and wish to acquire work experience to kick your careers in this area, apply & become a part of our team!

Activities:

·        To support the Regulatory Affairs team in maintaining registered products portfolio

·        To support local translation and dossier adaptation/to assist the preparation of submission dossier

·        To support activities related to the Health Authority TITCK database daily and inform the RA team accordingly

·        Prepare weekly analysis of TITCK registered product list

·        Becoming familiar with country regulations

·        To ensure the databases updated

·        To participate internal meetings, if needed

·        To prepare or maintain technical files as necessary to obtain and sustain product approval.

Qualifications

·        Being a 4th year or later undergraduate student in a Faculty of Pharmacy or Chemistry or Chemical Engineering

• Availability of a minimum of 3 days availability per week
• Willingness to learn and develop personal qualifications
• Strong verbal and written communication skills both in Turkish and English
• A strong sense of ownership and accountability
• Strong learning agility
• Experience in Microsoft Program

 

 

Required Skills:

 

 

Preferred Skills: