Our client, a pharmaceutical multinational is currently looking for a Technical Writer/Compliance Specialist to join their team in Limerick. This is initially a 12-month contract with a strong possibility of extension. Role and Responsibilities: Manage Deviations, CAPA, Change Control, Audits, and Quality risk manageme
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Documentation Co-Ordinator, Quality
Edwards Lifesciences
Shannon
7 days ago
Shannon
7 days ago
Provides clerical/administrative in support of Product Configuration Services (PCS) activities.Key Responsibilities:• Prepare and upload electronic documentation for Enterprise Change Requests• Create Enterprise Change Requests (ECR) in PLM under direction of management• Perform incorporation of approved changes to documentation
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Technical Writer/Compliance Specialist
QPTech
Co. Limerick, Limerick
3 days ago
Co. Limerick, Limerick
3 days ago
Our client, a pharmaceutical multinational is currently looking for a Technical Writer/Compliance Specialist to join their team in Limerick. This is initially a 12-month contract with a strong possibility of extension. Role and Responsibilities: Manage Deviations, CAPA, Change Control, Audits, and Quality risk manageme
Provides clerical/administrative in support of Product Configuration Services (PCS) activities.Key Responsibilities:• Prepare and upload electronic documentation for Enterprise Change Requests• Create Enterprise Change Requests (ECR) in PLM under direction of management• Perform incorporation of approved changes to documentation