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SIRE Life Sciences®

African Markets Regulatory Affairs Specialist


SIRE Life Sciences®

African Markets Regulatory Affairs Specialist

Location: Belgium

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Biotechnology and Pharmaceutical organization, based in Brussel Belgium.

The client is a strong player in the pharmaceutical field with a focus on Animal Health who puts effort in business relationships with customers.

ROLE DESCRIPTION

In this role you will be responsible for setting up a livestock in Africa for 1 year with possible extension.

RESPONSIBILITIES

- Manage the whole process in setting up this project in relation to RA activities
- Analyze potential new registrations and participate in decision making process
- You'll develop, implement en design a plan for new product registrations
- Work closely together with the other RA departments to ensure that the regulatory plan is fully aligned with business activities
- Oversight the budget
- Assist in the:
Submission and follow-up of Market Access Requests and requests for registration dossiers, certificates and product samples
Compilation, translation and submission of registration dossiers
Responses to questions and additional information

REQUIREMENTS

- Bachelor degree in a Chemistry, Pharmacy, Biology or Veterinary Medicine related discipline, or equivalent experience
- At least 5 years' experience of pharmaceutical, feed additive and/or vaccine Regulatory Affairs at a national or regional level
- Experience in the African markets is considered as a plus
- Ability to multi-task and to work to demanding timelines
- Ability to negotiate to obtain necessary resources and technical support
- Excellent communication skills (written and spoken English)

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.

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SIRE Life Sciences®

Job Description

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Biotechnology and Pharmaceutical organization, based in Brussel Belgium.

The client is a strong player in the pharmaceutical field with a focus on Animal Health who puts effort in business relationships with customers.

ROLE DESCRIPTION

In this role you will be responsible for setting up a livestock in Africa for 1 year with possible extension.

RESPONSIBILITIES

- Manage the whole process in setting up this project in relation to RA activities
- Analyze potential new registrations and participate in decision making process
- You'll develop, implement en design a plan for new product registrations
- Work closely together with the other RA departments to ensure that the regulatory plan is fully aligned with business activities
- Oversight the budget
- Assist in the:
Submission and follow-up of Market Access Requests and requests for registration dossiers, certificates and product samples
Compilation, translation and submission of registration dossiers
Responses to questions and additional information

REQUIREMENTS

- Bachelor degree in a Chemistry, Pharmacy, Biology or Veterinary Medicine related discipline, or equivalent experience
- At least 5 years' experience of pharmaceutical, feed additive and/or vaccine Regulatory Affairs at a national or regional level
- Experience in the African markets is considered as a plus
- Ability to multi-task and to work to demanding timelines
- Ability to negotiate to obtain necessary resources and technical support
- Excellent communication skills (written and spoken English)

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.

Additional Information

Last updated
Employment type
Full time
Contract type
Self employed
Number of vacancies
1
Min. experience
Two years
Min. education
Bachelor
Industry / category
Jobs in Research & Development (R&D)