7 Aug 2014

Regulatory Affairs Specialist – Africa Region Job Vacancy

Our client is an NGO with a mission to provide affordable access to high-quality reproductive health products for women and girls around the world through a sustainable value chain, empowering them to make and act on safe choices.

The overall purpose of the Regulatory Affairs Specialist is to:

  • Be responsible for the regulatory landscape assessment and meet with local stakeholders to support the registration activities in on-going project countries;
  • Responsibility for the compilation, regulatory accuracy, and completeness, of the documentation required by the Regulatory Authorities;
  • Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents;
  • Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.

Key Competencies and Qualifications:

  • Excellent employee relations skills;
  • Great team player with excellent collaboration skills;
  • Willingness to take on responsibilities and challenges;
  • Excellent communication skills, high English level proficiency;
  • Someone with a passion to make a difference in the lives of people.


  • Bachelor Degree in Science (Medicine, Pharmacy, Biochemistry etc.);
  • At least 2 years of experience with regulatory registrations of medical devices and/or drug products;
  • Basic knowledge of African regulatory requirements and GMP’s;
  • Excellent technical writing skills and computer literate;
  • Bilingual (English/French) is highly desirable.

How to Apply:
If you are qualified and up to the challenge upload your CV to and apply online by 5pm 8th August 2014

Please note that only qualified candidates will be contacted.Our client is an Equal Opportunity Employer

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