QA Validation Technical Writer

A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position.

Role of this position

• Execution of SIP/ cleaning and continuing validation protocols.
• Writing and approving Deviations/ GMP documents
• Technical writing experience in writing site reports.
• Generate/review/Approval of SIP/ CIP protocols
• Generation of Summary Reports
• Assessment of SIP/ CIP issues during study runs and closeout of deviations

JOB REQUIREMENTS

• Relevant 3rd level degree.
• Minimum of 2 years experience working in a GxP environment.
• Preferable to have experience in a commercial Biologics Manufacturing site.
• Experience in SIP/ cleaning validation results reporting review beneficial

N.B. It is essential that you hold a valid working visa for Ireland 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. 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.