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    Technical Writer - Cork, Ireland - Cpl Recruitment

    cpl recruitment background
    Description

    Key Deliverables:

    Supporting Pharmaceutical Manufacturing Operations and Technical groups to; Own document revision and routing on document management system and drive on time approval Design, update and improve facility/process procedures and business processes.

    Design, update and improve Manufacturing Batch Records.

    Design, generate and update Operations Area Logbooks Design, generate and update Training Documentation Design, update and improve EH&S systems and documentation.

    Design and generate PQ Protocols Design update/improve other documentations associated with the small and large molecule business Work with Technical groups in developing key technical documents to facilitate the start of a new facilitating and the introduction of the new products Opportunity to:
    Support a dynamic Small / Large Molecule manufacturing environment. Develop/learn key understanding of core manufacturing principles. Involvement in New Product Introductions. Deliver in innovative Manufacturing Areas. Support multiple manufacturing functions (Eng, Chemistry, QA, EHS)

    Key Attributes Relevant engineering/ science 3rd level qualification or operational experience PhD, Masters Chemistry very desirable Previous pharma production operations/ projects/process experience Strong sense of customer focus and teamwork Previously demonstrated flexibility and willingness to take on different job tasks Self motivated/ proactive approach with the ability to operate without close supervision Proven ability to deal with unexpected issues using problem solving skills Commitment to meet deadlines Right first time attitude Demonstrated technical writing skills in the generation of documents and high level of IT skills Good planning and organisation skills essential Skills:
    lab analyst scientific

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