AYRTON Drug has job opportunities in Ghana to recruit Regulatory Affairs Executive. We were incorporated On the 24th September 1965 by the Late Mr. Samuel Benson Adjapong. As a Ghanaian Entrepreneur and the first Ghanaian Chief Pharmacist at the Ministry of Health; he was issued a certificate to commence business on 21st October 1965. The company's journey to stardom began in a small plant in Kokomlemle a suburb of Accra with a tablet making machine and a staff of ten(10). It moved to its current location on the Abeka Road, Tesano also in Accra in 1969.
During the years 1970-1982, when many manufacturing companies in Ghana were operating on the margin due to the harsh economic conditions, Ayrton kept alive the hope of becoming a force in the pharmaceutical industry in Ghana with a about 30 product lines.
JOB SUMMARY |
Company: | AYRTON Drug |
Industry: | Pharmaceutical |
Category: | Quality Assurance |
Location: | Accra |
Job Status: | Full-time |
Salary: | GH¢ |
Education: | Undergraduate |
Experience: | 2 years |
Job Expires: | 10 Jun, 2013 |
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
Required Skills or 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
NB: SALARY & BENEFITS : VERY ATTRACTIVE
Interested applicants should send applications to include CV to:
adml2@hotmail.com
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