Regulatory Affairs Specialist – Saudi Arabia Riyadh
Would you like to work for a rapidly growing international healthcare company?
Do you consider you have the right experience for a Regulatory Affairs Specialist role? If yes then send us your resume and enter the recruitment process right away!
Join Covidien where we appreciate your talent experience and passion for your work. You can count on professional and personal development exciting challenges and a dynamic environment.
As a Regulatory Affairs Specialist in Covidien you will be responsible for ensuring that our company and our products are complying with the local medical devices regulations. You will be working very closely with our local marketing team as well as local distributors to secure compliance of our products. As a result we will be able to place our products in the market and also remain in compliance with the local law.
In return we’ll provide great training and development opportunities as well as an excellent benefits package. It’s a unique opportunity to be part of a rapidly growing company like Covidien.
Our Regulatory Affairs Specialist is expected to be located already or willing to locate in Riyadh.
Principal Accountabilities of Regulatory Affairs Specialist• Work closely with local and regional marketing team to ensure that we have our products registered according to their launching plan
• Work closely with distributors to make sure that they have all the necessary regulatory documents
• Follow up field safety corrective actions initiated by Covidien with distributors and the competent authority
• Work closely with the marketing team in tender preparation
• Work closely with marketing quality and end customers in complaints handling
• Submit the needed regulatory certificates to the competent authority to make sure that all our products are having the needed marketing authorization
• Maintain the registration certificates valid and renew them whenever expired
• Support any local regulatory projects.
Skills
Skills Qualifications
• 0 – 3 years’ experience in medical devices Pharma regulations management
• BSBA Degree in Biomedical engineering Business Administration Pharma logistics
• Relevant experience of leading projects workshops or process improvements
• Excellent problemsolving and analytical skills
• Fluency in both written and spoken English
• Excellent software skills especially office programs
• Excellent written and verbal communication skills
• Selfmotivated and proactive
• Ability to manage conflict effectively.
This job is posted in the following Specialties
Regulatory Affairs Pharmaceutics Medical Law Medical Devices