A QA Validation Technical Writer is required by Careerwise Recruitment to work for our Limerick based biopharma client.
Role of this position
- 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
- 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 email@example.com
CareerWise Recruitment (In Search of Excellence)