Description
A Global generic pharmaceutical company based in Dublin is currnelty recrutiing for a QC Analyst.Main Objectives:
- To carry out analytical testing on Raw Materials and Finished Products.
- To provide technical support as required by management
Main Duties:
- Analyse Raw Materials, In-Process Materials and Finished Products.
- To maintain all laboratory notebooks, records, chromatograms to an acceptable GLP standard.
- To maintain good housekeeping and hygiene within the laboratory.
- To maintain and follow all relevant Standard Operating procedures.
- To calibrate and maintain designated laboratory instruments.
- To support the laboratory testing schedule in order to achieve an efficient QC system.
- To bring to the notice of the supervisor or manager any discrepancies, deviations or non-conformance's in testing or work practice.
- To follow up to date analytical practices with reference to pharmacopoeias, specifications, regulations and industry standards.
Requirements:
- Minimum of 1 year of HPLC experience within a highly regulated laboratory environment (IMB/FDA)
- Recognized 3rd level science qualification (preferably chemistry / pharmaceutical based)
- Proven technical ability in laboratory systems.
- Ability to work flexible shift hours if required.
If you would like to here more about the company and role please contact me Anna Mooney or apply below with an up to date CV.