Quality Control Analyst
The Quality Control Analyst role is to carry out analytical testing on finished product & raw materials using the approved procedures in order to comply with cGMP, Health and Safety, SOPs and environmental and regulatory requirements while ensuring to meet  customers needs
-     Maintain and follow all relevant Standard Operating Procedures (SOPs).
-  Adherence to the existing methods with reference to pharmacopoeias, specifications, regulations and industry standards.
-  Adherence to regulatory and industry compliance and data integrity expectations.
-  Displays technical competency and full understanding of methods and equipment relating to the following areas: HPLC, UPLC, GC, IR, UV, ICP, particle size, dissolution & physical testing.
-     Full analysis of raw materials in a timely manner using appropriate analytical techniques with limited analyst related OOS.
-    Full analysis of finished product (tablets, boluses, veterinary drenches etc) in a timely manner using appropriate analytical techniques with limited analyst related OOS.
-   Full analysis of contract manufactured products in accordance with customer specifications with limited analyst related OOS.
-   Incoming inspection of foils, labels, bulk finished goods and injectables.
- Calibration and maintenance of laboratory equipment as per calibration procedures.
-    To support the laboratory testing schedule in order to achieve an efficient QC system and Customer Service level of >95%.
-    To maintain all laboratory logbooks, notebooks & associated documentation to GLP.
-  Liaise with team leader/supervisor & production so that timely reporting of results is achieved.
-    Ensure timely feedback of all queries as appropriate.
-  To bring to the notice of the team leader/supervisor any discrepancies, deviations or non-conformances in testing or work practice.
-     Display ability and follow up on Corrective Actions.
-     Sending out samples for external analysis when requested.
-     Participating in internal/External Audits.
-      Liaising with external suppliers/vendors in relation to QC consumable s.
-  -  Ensure existing quality procedures are followed and where appropriate suggestions/change control forms are prepared so that the quality system will be continuously improved.
-     -   To adhere to any agreed internal laboratory rota tasks.
-  Adherence to laboratory safety measures at all times highlighting areas for improvement
-       - Ensuring that laboratory is kept tidy and that GLP/GMP standards are adhered to at all times
-     -  Bachelor&rsquos degree in a science-based discipline with a minimum of 6 years&rsquo experience in a pharmaceuticals.
-      - Experience working within a pharmaceutical cGLP Environment with knowledge of EU GMP and US FDA Guidelines
If you are interested in this role as a Quality Control Analyst please click on the apply button and send us your CV"
You can also contact our office on 093 41932 to discuss this opportunity in further detail
"If you would like to learn more about our company please visit our website" www.bdr.ie