Technical Writer

An experienced Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client.

THE ROLE:

• Collaborate with subject matter experts and key functional department personnel to ensure timely development and accurate content of GMP documents (e.g. standard operating procedures, system design documents, and work instructions).
• Perform retrospective assessment of computerized system administration activities and author the resulting reports.
• Maintain an awareness and understanding of current site document requirement, document control procedures, and good documentation best practices. Review internal GMP documents to ensure they are compliant with these expectations and suggest improvements.
• Manage and coordinate activities related to document creation using the Electronic Document Management System, including document initiation, workflow support, revision, and retirement.
• Conduct compliance review of electronic work tickets for adherence to Good Documentation Practices/Requirements.

REQUIREMENTS:

• BS/BA in Life Sciences, Engineering, English or related field.
• 5 years of relevant experience or equivalent combination of education and experience.
• Strong knowledge of Good Documentation Practices (ALCOA), ISPE Standards, GAMP5, and Documentation Management/Life Cycle guidance.
• Strong writing and proofreading skills in a technical and scientific capacity.

Please call Michael O’Connor today for further information on 091-452410 or email moconnor@careerwise.ie

CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors.

We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.

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