Pharmaceutical QA Lead

5 days ago


Dublin, Dublin City, Ireland CPL Full time

Requirements

  • A Bachelor's or Master's degree in Chemistry or a related scientific field is required, with ideally a minimum of 10 years of experience in the pharmaceutical industry, preferably in a Quality Assurance role.
  • The Quality Assurance Lead Specialist must possess strong initiative and be capable of working both independently and collaboratively within a team.
  • The ideal candidate will demonstrate proficiency in the following areas:
    • Experience in API manufacturing from NPI through to commercialisation (end to end product lifecycle).
    • In-depth knowledge of cGMP principles relevant to API manufacturing.
    • Knowledge of regulatory requirements, trends, hot topics and emerging requirements.
    • Strong awareness of the CDMO business environment and financial acumen.
    • Exceptional time management and organizational abilities, coupled with a track record of effectively handling multiple tasks and customers simultaneously.
    • Excellence in communication, collaboration, working with minimum direction, 'can do, solutions orientated' attitude, leadership, problem solving and driving continuous improvement.
    • Proficiency in interpreting industry regulations and identifying potential gaps in current site and QA procedures.
    • Capacity to manage numerous projects concurrently and meet strict deadlines.
    • Strong troubleshooting skills and a sound technical background in quality within the pharmaceutical manufacturing sector.

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