Great opportunity for a Technical Writer to join our team with our biotech client in Limerick to support the document preparation and review activities for their Cleaning Validation Program.
o Generating a Validation Protocols.
o Generate/review/Approval of CV/ SIP protocols,
o Generate Reports
o Maintain and update Cleaning/ Steam in place Validation Plan
o Schedule of cleaning/SIP activities with Manufacturing
o Actively look for Continuous improvements
o Liaise with numerous departments
QUALIFICATIONS and EXPERIENCE:
o BSc or BEng
o 3+ years Biotech experience in Validation specifically cleaning/SIP validation
o Good technical knowledge of BioTech equipment and the concepts of BioTech manufacturing.
o Experienced Technical writer,
o Experience in Deviation/Change control writing,
For full details on this role please contact Kathy on 021 4777329 or email@example.com or apply directly through this advert.