- Review/implementation of QMS 
    - Ensure GMP & GLP compliance and documentation
    - Handling of deviations, change controls, non-conformances
    - Manage critical quality parameters 
    - Develop effective mechanism for investigations and analytics
    - Conduct GMP audits
    - Coordination with other functions and regulatory auditors
    - Contribute in solving queries from regulatory authorities

    M.S. in Analytical Chemistry, Chemistry, Microbiology, Pharmaceutical Sciences or equivalent with multiple years of pharmaceutical experience
    Understanding of pharmaceutical manufacturing and packaging operations of large volume parenterals
    We are looking for an effective and team-oriented leader with hands-on experience in controlling QA, QC chemistry and QC Microbiology

    Experience in 
    - Quality Management System
    - Large Volume Parenterals
    - developing SOPs, protocols and technical documents
    - Deviation management and batch disposition
    - Validation and qualification activities
    - Auditing and authority inspections
    - Experience in QC Microbiology is preferable

    10+ years experience

    Recruiter Name:Fredrik
    Email Address:frederic.dovi-akue@dopharma.net

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