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    QA Manufacturing Specialist

    Dún LaoghaireContractCompetitive
    Back to job search
    4 weeks ago
    JN -052026-2002404

    QA Manufacturing Specialist

    Dún Laoghaire Contract Competitive

    QA Manufacturing Specialist

    About the job

    Description:

    The Manufacturing Specialist (Investigation Lead) will be primarily responsible for leading investigations for fill/finish/inspection and packaging deviations. Specialists will also be involved in applying process, quality, compliance, and analytical knowledge to complete the following:

    • Manage deviation investigations, including establishing investigation teams, leading root cause analysis, development of CAPAs, completing product impact assessments and writing comprehensive compliant documentation of all findings.
    • Clear and concise technical writing of complex investigations
    • Drive improvements to the investigation process
    • Present investigations to regulatory inspectors and internal auditors
    • Clearly communicate investigation progress to impacted areas and leadership
    • Coordinate and lead cross-functional teams through complex investigations, and complete tasks on-schedule.
    • Project management of the investigations end to end
    • Present complex topics to large and small groups at various levels and quickly understand and clearly communicate complex issues.
    • Build effective relationships across functions.
    • Navigate through ambiguity and provide a structured problem-solving approach.
    • Able to apply inductive and deductive reasoning in the investigation process

    Qualifications:

    • Bachelor's Degree in Science or Engineering and 5+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (ie process development, engineering, quality) OR * Associate's Degree in Science or Engineering and 8+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (ie process development, engineering, quality) * 10+ years directly related experience in a biotech/pharma manufacturing or manufacturing environment
    • Detailed technical understanding of fill/finish operations
    • Experience with compliance, problem-solving, root cause analysis, critical thinking, project management, and quality systems.
    • Experience leading complex investigations
    • Experience participating in and leading cross-functional teams
    • Experience in managing multiple, competing priorities in a fast-paced environment
    • Experience presenting to inspectors during regulatory inspections and internal audits.
    • Excellent technical writing
    • Excellent presentation and communication skills, ability to communicate and collaborate with technical and management staff
    • Ability to be flexible and manage change

    © 2026 Morgan McKinley
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