Manufacturing Specialist

    Dún LaoghaireContractCompetitive
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    2 hours ago
    JN -032026-1999048
    New

    Manufacturing Specialist

    Dún Laoghaire Contract Competitive

    About the job

    *12 Month Contract - High possibility to Extend*

    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