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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.

Requirements:

  • 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 http://www.altimaafrica.com/careers.php 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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