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:
1. Provide analytical services and support to site.
2. 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.
3. Maintain, and update methods, specifications and SOP’s in compliance to pharmacopoeia and regulatory requirements.
4. Update the QC Team Leader on potential problems and highlight improvements where possible by use of the normal communication menus.
5. Ensure all quality documentation and records are complete and current.
6. Ensure QC laboratories meet current Good Laboratory Practice (cGLP) requirements.
7. Ensure relevant procedures are correctly defined and followed.
8. Ensure that equipment used for analysis is within calibration.
9. Audit and review test results on a daily basis and ensure compliance with cGLP.
10. Completion and maintenance of notebooks and analytical reports as required.
11. Ensure compliance to cGMP at all times.
For more information and a confidential chat, feel free to reach out to me.
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