A key role within our pharmaceutical company in County Waterford has become available.
We are seeking an analytical services expert to support our site.
Key Responsibilities:
* To provide analytical services and support to the site.
* To effectively interact with other departments on matters related to raw materials, intermediates, and finished batch releases. This includes maintaining close contact with Quality Assurance, Production, Engineering, and Planners.
* To maintain and update methods, specifications, and Standard Operating Procedures (SOPs) in compliance with pharmacopoeia and regulatory requirements.
You will be responsible for updating the QC Team Leader on potential problems and highlighting improvements where possible through normal communication channels.
All quality documentation and records must be complete and up-to-date.
* To ensure that the QC laboratories meet current Good Laboratory Practice (cGLP) requirements.
* To ensure that relevant procedures are correctly defined and followed.
* To ensure that equipment used for analysis is calibrated as required.
* To audit and review test results daily and ensure compliance with cGLP.
* To complete and maintain notebooks and analytical reports as necessary.
Ensuring compliance with Current Good Manufacturing Practice (cGMP) at all times is also a critical aspect of this role.