Reports to Managing Director

Scope:
The role of Regulatory Affairs Executive is to ensure that the drug regulatory aspect of the business is well developed and maintained.

Responsibilities:

•  Develop registration strategies, prioritize assignments, co-ordinate regulatory projects and activities in accordance with the strategic objectives of the company
•  Review, analyze and co-ordinate data for new product submissions, line extensions and  variations to marketed products
•  Preparing regulatory documentation and dossiers
•  Keep accurate records on the usage of narcotic and psychotropic substances by the company, applying for narcotic licence and submission to appropriate bodies.
•  Ensure full regulatory compliance to all local and international regulations, codes and standards.
•  Liaising and building relationships with regulatory authorities
•  Writing clear, accessible product labels and patient information leaflets
•  Project managing teams of colleagues involved with the development of new products, variation of products, artwork designing and approvals.
•  Analyzing and communicating trends in regulatory legislation, guidelines and customer practices in all the countries that the company exports to and their implications to the company

Qualification Required & Experience

•  University qualifications in Pharmacy or related Science discipline are essential.
•  At least 2 years experience with Drug Regulatory Affairs is preferred
•  Experience working on both local and foreign drug dossiers is preferred.
•  Competencies
•  Excellent communication skills
•  Ability to work and deliver results with very little supervision
•  Attention to detail
•  Excellent presentation and negotiation skills
•  Good organization and analytical skills
•  Equity statement
•  Ability to develop productive working relationships

SALARY &  BENEFITS :  VERY ATTRACTIVE

Location: Accra

How To Apply For The Job

Applications should be sent to:

adml2@hotmail.com  

Closing Date: 10 June, 2013