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Regulatory Affairs - Veterinary Product & Feed Additive

Remote: 
Full Remote
Contract: 
Experience: 
Entry-level / graduate
Work from: 

Offer summary

Qualifications:

Degree in Veterinary, Life Sciences, Pharmacy, or related field, 1-3 years experience in Regulatory Affairs is a plus, Knowledge of EU & UK Healthcare Regulations.

Key responsabilities:

  • Prepare regulatory documentation and registration dossiers
  • Analyze and share regulatory trends, manage label design
  • Support safety department in materials preparation
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Michael page Human Resources, Staffing & Recruiting Large https://www.page.com/
5001 - 10000 Employees
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Job description


  • Healthcare - Lifesciences - Pharma - Veterinary medicines - Feed additives | Regulatory Affairs Specialist - EU & UK Regulations - Regulatory registration


About Our Client

Our client is a fast- moving large-scale pharmaceutical company with over 3000 employees and an international presence in more than 20 countries. They have a significant impact on the Life Sciences sector and are renowned for their commitment to innovation, development and quality. Strong growing ambitions are expected over the 5 coming years.

Job Description

As a Successful Regulatory Affairs Specialist - Veterinary products and Feed Additives, you will have the following responsibilities:


  • Prepare various regulatory documentation for veterinary products and feed additives.
  • Prepare registration dossiers for veterinary products and feed additives.
  • Submit registration documentation to competent authorities worldwide & monitor progress.
  • Analyse, understand and share relevant regulatory trends related to the Veterinary medicines and the feed additives (Focus on EU & UK).
  • Manage the label design of the veterinary products and feed additives.
  • Support safety department in their materials preparation.


The Successful Applicant

As a Successful Regulatory Affairs Specialist - Veterinary products and Feed Additives, you have the following profile


  • A degree in Veterinary, Life Sciences, Pharmacy, or a related field.
  • 1-3 years of experiences in a previous Regulatory Affairs position is a plus.
  • Knowledge of EU & UK Regulations within the healthcare industry.
  • Excellent communication skills - both oral and written - to liaise with various departments and regulatory bodies.
  • A strong eye for detail, ensuring all regulatory documents are accurate and complete.
  • Capacity to work independently with the ability to analyse and interpret complex regulatory documentation.
  • A strong cooperative mindset to liaise and collaborate with the different departments (Safety, Clinical, Marketing ...).
  • Fluent in English, Dutch being a plus.
  • Willingness to work at the Antwerp office most of the time.


What's on Offer

As a Successful Regulatory Affairs Specialist - Veterinary products and Feed Additives, you will have:


  • A competitive fix salary coupled with interesting benefits package
  • A vibrant and innovative work culture in the Life Sciences department.
  • Opportunities for professional development within a growing international pharmaceutical company.
  • Working in a prominent location in Antwerp.

Required profile

Experience

Level of experience: Entry-level / graduate
Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
English
Check out the description to know which languages are mandatory.

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