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Manager, R&D QA, Global Audit, Inspections and R&D Quality

Job in Marlow, Buckinghamshire, SL7, England, UK
Listing for: Kyowa Kirin International plc.
Full Time position
Listed on 2025-12-30
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist
Job Description & How to Apply Below

Manager, R&D QA, Global Audit, Inspections and R&D Quality

Join to apply for the Manager, R&D QA, Global Audit, Inspections and R&D Quality role at Kyowa Kirin International plc.

Overview

At Kyowa Kirin International (KKI), our purpose is to make people smile. We embed care into everything we do and deliver life‑changing solutions sooner. Our culture is rooted in Teamwork, Commitment to Life, Innovation, and Integrity.

Job Purpose

The Manager, R&D QA, Global Audit, Inspections and R&D Quality is responsible for managing Quality Assurance systems, processes and conducting internal and external audits and reviews, training, and reporting according to KK standards. The R&D QA Manager will support the QA program to assure the accuracy and quality of scientific data submitted to regulatory agencies in support of new drug applications and/or biological licensing agreement applications.

The R&D QA Manager will collaborate and provide key quality input to KK’s R&D function.

Responsibilities
  • Acts as key point of contact for GCP/GLP quality issues reported by KK staff and provides ongoing feedback to management on potential quality-related risks. Involvement in clinical trials includes, but is not limited to, independent review and approval of deviations and CAPAs, GCP guidance, and quality agreement preparation.
  • Develops and delivers GCP-related training to KK staff as needed.
  • Performs, reports assigned GCP/GLP audits of KK studies, including but not limited to, clinical investigator sites, vendor/CROs, internal system/processes, clinical data and documents, as applicable.
  • Prepares timely well‑written reports, obtains/evaluates audit responses and oversees tracking mechanism for QA audits and manages CAPA as per KK standards.
Qualifications
  • Bachelor’s degree required and in science/life sciences preferred.
  • Strong experience in drug development and 3+ years of experience in GCP/GLP Quality Assurance including detailed knowledge of EMA, FDA, MHRA, ICH regulations and other applicable regulatory requirements.

Kyowa Kirin International is an equal opportunities employer.

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