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Elanco

Global animal health pharmaceutical company

Qualified Person

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDublin, IrelandNo salary listed

About the Job

Requirements

  • Qualified Person status for veterinary medicinal products in accordance with Regulation 2019/6 and applicable veterinary Good Manufacturing Practice requirements.
  • A minimum Master’s degree in a relevant scientific discipline.
  • At least two years of experience in a Quality department within a pharmaceutical site, or equivalent.
  • Demonstrated knowledge of pharmaceutical regulations, Good Manufacturing Practice and Good Distribution Practice.
  • Working knowledge of Microsoft Office, Veeva and SAP.

Responsibilities

  • Conduct technical reviews and certify European finished-product batches in accordance with Regulation 2019/6, Regulation (EU) 2025/2091 and applicable EU Good Manufacturing Practice requirements, including Articles 39 and 40.
  • Manage quality documentation and act as the primary contact for the European Manufacturing and Quality organisation regarding European batch releases, service-quality indicators, deadlines and follow-up actions.
  • Assess critical deviations with relevant stakeholders and support recall decisions, including participation in management notification processes and product-related governance meetings.
  • Maintain and improve the Elanco Ireland quality system by preparing and approving procedures, work instructions, site master file content, Qualified Person declarations and other product-supporting quality documents.
  • Manage change controls, deviations and self-inspections for the Elanco Ireland entity, support audits and inspections, communicate potential market issues to authorities, and share knowledge of European Union pharmaceutical quality expectations across the organisation.

Desired Qualifications

  • Experience with veterinary medicinal products and European batch release activities.
  • Practical experience managing quality systems, including change controls, deviations and self-inspections.
  • Experience supporting regulatory authority inspections, audits or market issue notifications.
  • Experience preparing quality documentation such as procedures, work instructions, site master file content or Qualified Person declarations.
  • Experience working with cross-functional European quality organisations and communicating quality information in English.

About the Company

Elanco

Global animal health pharmaceutical company

Elanco is a global animal health company that develops and sells medicines, vaccines, and preventive care products for livestock and pets. Its portfolio includes prescription medicines, vaccines, parasite controls, and other welfare products used by veterinarians, farmers, and pet owners to prevent or treat disease and improve wellbeing. Since becoming independent after separating from Eli Lilly and acquiring Bayer Animal Health in 2020, it ranks as the world’s second-largest animal health company with a broad, globally distributed product line and direct-to-consumer capabilities. Its goal is to improve animal health and welfare worldwide by providing effective, accessible products and services while growing sustainably.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Indianapolis, IN
Founded
1954

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