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Vetoquinol

Develops and markets veterinary medicines

Principal Scientific Officer - Regulatory Writing, Safety and Efficacy

Regulatory & Quality (Life Sciences)Posted on Nov 3
Full-timeMagny-Vernois, FranceNo salary listed

About the Job

Requirements

  • A scientific doctorate with a specialization or equivalent is required.
  • At least 10 years of experience in drug development is required.
  • Proficiency with dedicated computer tools is required.
  • C1-level English is required.
  • The role calls for openness, analytical and synthesis skills, and the ability to make proposals.

Responsibilities

  • Define and propose the development plan for the Safety and Efficacy sections, including studies needed to achieve the approved Target Product Profile, in collaboration with relevant contributors.
  • Construct and write regulatory sections documenting efficacy and safety, ensuring compliance with applicable regulations.
  • Lead the strategy for responding to regulatory authorities’ questions about submitted efficacy and safety sections.
  • For preliminary projects, propose actions to assess and select projects and actively participate in designing development plans.
  • Define project development rationales, assess acquisition opportunities, and analyze scientific communications.
  • Represent the Preclinical and Clinical Department on project teams and coordinate implementation of actions defined for product development.
  • Coordinate development-plan actions within the Preclinical and Clinical Department, ensuring completion on time, coordinating corrective actions to meet critical milestones, and keeping the project team informed.
  • Ensure communication and information flow between the project team and the department’s team leads.
  • Help translate the expected attributes of the Target Product Profile into the target product characteristics and update them based on project data.
  • Participate in scientific communication within and outside the company, sharing information across departments and developing the company’s external profile.
  • Participate in or facilitate multidisciplinary expert working groups to serve the company’s interests.
  • Attend conferences and monitor scientific literature in line with company strategy to stay current in veterinary development.
  • Represent and advocate for the company with professional organizations and at professional events, including publications and conferences.
  • Collaborate with the company’s Group, US, and Brazil divisions and the Medical Marketing Department.
  • Collaborate with external partners, contract research organizations, key opinion leaders, regulatory authorities, and professional organizations.

About the Company

Vetoquinol

Develops and markets veterinary medicines

Vetoquinol is a global animal health company that develops and markets medicines and health products for pets and livestock. Its products are used to treat diseases, prevent illness, and support animal well-being, distributed through a network of subsidiaries and partners in about 24 direct countries with products available in around 100 countries. Core operations include research, development, and commercialisation of veterinary pharmaceuticals and health solutions for both companion and farm animals. What sets Vetoquinol apart is its long family-led history and steady international expansion, including an IPO in 2006 to accelerate growth, which has helped it build a widespread, multi-country presence. The company’s goal is to improve animal health globally by bringing effective veterinary products to markets around the world and expanding access through direct operations and partnerships.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Paris, France
Founded
1933

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