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Job Title

QA Validation Technical Writer






A QA Validation Technical Writer is required by Careerwise Recruitment to work for our Limerick based biopharma client. THE ROLE: * Generate/review/Approval of SIP/ CIP protocols. * Generation of Summary Reports and strong quality background essential. * Ability to work on own initiative. * Maintain and update Cleaning/ SIP Validation Plan. * Schedule of Cleaning/ SIP activities with Manufacturing. REQUIREMENTS: * Experienced Technical writer. * Experience in Deviation/Change control writing. * Experience in continuing validation and generation of assessments for continuing. * Experience on writing and approving Deviations/ GMP documents. Please call Michael O'Connor today for further information on 091-452410 or email 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. By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent.

Date Added

264 days ago