Search Results: 8 vacancies
...The Role:
Technical Writer
Limerick – Onsite
Permanent or Contract Opportunity
Role Brief:
Perform all technical writer related tasks necessary for the creation and maintenance of quality GMP documentation in support of the Technical Operations Engineering...
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...
...Manufacturing design and process understanding.
Good working knowledge of Solidworks and/or Pro Engineer CAD.
Strong technical writer.
Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device...
...Validation specifically cleaning validation
Experience in assessment of cleaning issues during study runs,
Experienced Technical writer,
Experience in Deviation/Change control writing,
Capable of managing a large program, so project management skills would be...
...Validation specifically cleaning validation.
Experience in assessment of cleaning issues during study runs.
Experienced Technical writer.
Experience in Deviation/Change control writing.
N.B. It is essential that you hold a valid working visa for Ireland
Please call...
...knowledge of Solidworks and/or Pro Engineer CAD.
Good presentation skills (working knowledge of MS PowerPoint).
Strong technical writer.
Attention to detail and Quality focus.
Good working knowledge of medical device quality & regulatory systems and medical device...
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Technical Writer – Cleaning Validation
Industry : BioPharmaceutical
Summary of Role :
Experienced Technical Writer.
Experience in Deviation...
QA Resources
Limerick
4 days ago
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IT Compliance Analyst (Technical Writer)
Industry : Pharmaceutical
Department: Information Systems
Role Summary:
The IT Compliance Analyst is responsible for ensuring...
QA Resources
Limerick
5 days ago
