Our client, a global pharmaceutical and veterinary trading company with Headquarters in Europe is looking for an experienced Pharmaceutical and Veterinary Drug Regulatory Affairs Consultant
Job Ref MN 6090
The Regulatory Affairs Consultant will be reporting to the Medical Director in Kenya and Europe and will be working with the Sales and Marketing Department in Kenya.
Job Profile
- In depth understanding of the different registration processes with the Ministry of Health and the PCPB.
- Understanding of the local regulations and methodology.
- Monitors and implements the changes in the Regulatory environment.
- Communicates with the other departments on all relevant regulatory and marketing issues.
- Registration files, in collaboration with RA-Officer:
- Prepares, compiles and approves registration files for submission
- Follows-up on status of registration files (including 5-yearly renewals)
- Uses expertise to improve updating process and timely approvals.
Person Profile
- Bachelors degree in pharmacy, veterinary or other related field.
- Registered with relevant regulatory bodies
- Work experience in pharmaceutical or veterinary field is an advantage
- 10 years work experience in pharmaceutical or veterinary field.
- Good communication and reporting skills.
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