A key role has become available in a leading pharmaceutical company based in County Waterford. The position entails providing analytical services and support to the site.
The ideal candidate will be responsible for maintaining effective interactions with other departments, particularly Quality Assurance, Production, Engineering, and Planners, regarding raw materials, intermediates, and finished batch releases.
Key Responsibilities:
* Maintain and update methods, specifications, and Standard Operating Procedures (SOPs) in compliance with pharmacopoeia and regulatory requirements.
* Update the QC Team Leader on potential issues and suggest improvements through regular communication.
* Ensure all quality documentation and records are up-to-date and complete.
* Verify that QC laboratories adhere to current Good Laboratory Practice (cGLP) requirements.
* Evaluate and maintain relevant procedures to guarantee adherence to cGLP.
* Confirm that equipment used for analysis is calibrated correctly.
* Daily review of test results to ensure compliance with cGLP.
* Complete and maintain notebooks and analytical reports as necessary.
This role requires strict adherence to Current Good Manufacturing Practice (cGMP) at all times.