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 Drugs kept alive the hope
of becoming a force in the pharmaceutical industry in Ghana with a about 30
product lines.
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JOB SUMMARY
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Company:
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AYRTON Drug
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Industry:
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Pharmaceutical
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Category:
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Quality Assurance
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Location:
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Accra
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Job Status:
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Full-time
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Salary:
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GH¢
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Education:
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Undergraduate
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Experience:
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2 years
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Job Expires:
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10 Jun, 2013
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Job Description
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:
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
How To Apply
Interested
applicants should send applications to include CV to:
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