A great opportunity to join a large and growing pharmaceutical company in County Waterford!
Details on the role below, if you are interested apply today!
Description:
• Provide analytical services and support to site.
• Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases. In particular, close contact maintained with Quality Assurance, Production, Engineering and Planners.
• Maintain, and update methods, specifications and SOP’s in compliance to pharmacopoeia and regulatory requirements.
• Update the QC Team Leader on potential problems and highlight improvements where possible by use of the normal communication menus.
Ensure all quality documentation and records are complete and current.
• Ensure QC laboratories meet current Good Laboratory Practice (cGLP) requirements.
• Ensure relevant procedures are correctly defined and followed.
• Ensure that equipment used for analysis is within calibration.
• Audit and review test results on a daily basis and ensure compliance with cGLP.
• Completion and maintenance of notebooks and analytical reports as required.
Ensure compliance to cGMP at all times.
For more information and a confidential chat, feel free to reach out to me on [email protected] or call me on 01-482 5494