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Regulatory Affairs Specialist

Remedial Health (YC W22)

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Job Description/Requirements

About Us

Remedial Health (YC W22) in Lagos improves access to medicines for healthcare retail businesses by providing direct access to manufacturers/registered distributors. Using technology, we offer just-in-time stock delivery, financing, and a wide selection of inventory to large pharmacies and remote chemist/PPMVs. Our focus is on enhancing business-to-business access to essential medicines.


About the Role

This is a full-time on-site role for a Regulatory Affairs Specialist at Remedial Health. The Regulatory Affairs Specialist will be responsible for ensuring compliance with regulatory requirements, preparing and submitting regulatory documentation, and managing regulatory affairs processes on a daily basis in Lagos.


Job Description

• Obtaining registrations of new medicines and maintaining existing registrations of medicines

• Manage the preparation of regulatory documents, dossiers and applications to enable the launch an maintenance of new products in the market whilst aligning and complying to regulations

• Analyze regulatory issues and communicate with relevant stakeholders

• Build relationships with key stakeholders and represent Kessington Global in an appropriate manner with regards to the values of the company

• Support the development of the strongest advertising and product promotion initiatives to ensure they’re within the regulations and ensuring identified risks are appropriately addressed and communicated.

• Work closely with other functions such as the Marketing and Supply chain units

• Provide support for market access (admission of medicines into the market alongside legal requirements for the logistical delivery of medicines to pharmacies and wholesalers 


Qualifications

  • Bachelor's degree in Pharmacy, Pharmacology, Biochemistry or any related field
  • Minimum of 2 years’ experience in regulatory affairs
  • Knowledge of pharmacology is an added advantage
  • Experience in preparing Regulatory Documentation and Submissions
  • Knowledge of Regulatory Requirements in the Pharmaceutical space is mandatory
  • Bachelor's degree in Pharmacy, Regulatory Affairs, or related field


Skills

  • Good verbal and written communication
  • Strong negotiation skills
  • Strong attention to detail and analytical skills












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