Vacancy: Regulatory Affairs Specialist - Africa Region
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:
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.
- 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 towww.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