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Elanco

Global animal health pharmaceutical company

Advisor, Quality Assurance - R&D Technical Development

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSpeke, Liverpool, UKNo salary listed

About the Job

Requirements

  • A Ph.D. in Life Sciences or a Master's degree with relevant equivalent experience in a technical area such as Pharmacy, Biology, Biotechnology, or Chemistry.
  • At least 5 years of experience in Quality Assurance, Quality Control, or a related technical field such as Pharmaceutical Development, Manufacturing, or Chemical Engineering.
  • Expert knowledge of Good Manufacturing Practice (GMP), global regulatory requirements such as FDA/CVM, EMA, MHRA/VMD, CMC-related activities, and R&D Quality Assurance from development through registration.
  • Ability to interpret complex regulations and policies, influence without authority, and drive favorable quality outcomes across multidisciplinary project teams.

Responsibilities

  • Provide quality leadership and GMP compliance guidance across global R&D teams, project groups, and contract manufacturing organizations (CMOs) to support product development, technical transfers, registrations, and launches.
  • Partner cross-functionally to shape quality strategy and ensure alignment with company standards and global regulatory requirements.
  • Implement and optimize quality systems, tools, and training tailored to technical development activities.
  • Serve as a global quality expert across R&D and project teams, set quality strategies, resolve complex compliance challenges, and develop and deliver compliance training.
  • Drive quality oversight for Computer System Validation (CSV), AI governance, electronic lab notebook (ELN) implementation, and equipment commissioning (IQ/OQ/PQ) to ensure digital tools and systems meet GxP and regulatory standards.
  • Conduct scientific and compliance reviews of CMC, preclinical, and clinical documentation; oversee material release for drug substance and product; and lead inspection readiness for regulatory authorities.
  • Manage qualifications, audits, corrective and preventive action (CAPA) reviews, and Quality Agreements for external partners, including CMOs, contract research organizations (CROs), and third-party organizations (TPOs).
  • Champion global R&D Quality Plans, self-inspections, quality metrics, and adherence to global quality, health, safety, and environment (HSE), and ethics standards.

Desired Qualifications

  • Background in vaccine or animal health and/or biotherapeutics (large molecule) development.
  • Experience in equipment qualification, including plans, test scripts, and summary reports, and computerized system validation (CSV) with IT/Engineering.
  • Experience designing or maintaining R&D Quality Systems, standard processes, and compliance training programs.
  • Skill in quality risk-assessment methodologies.
  • Auditing experience.

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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