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QC Finish Product Analyst

Quality & Laboratory
Glen Scheiner
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Job Reference: JO-2207-66280_1658847710


Do you have 1 plus years pharmaceutical experience in a GMP regulated environment? My Cork based client have an opportunity for a QC Finished Product Analyst to join their expanding team on a Permanent basis. The ideal candidate will be highly motivated with the ability to work in a fast-paced environment. If this sounds like the opportunity for you, please read on!


  • Carry out routine analysis on Finished Product samples ensuring compliance with cGLP/cGMP and that turnaround times are met. The testing carried out includes but is not limited to: HPLC, Osmolality, Organic Iodine, Inorganic Iodine, Thin Layer Chromatography.
  • Perform routine instrument calibration checks at appropriate times.
  • Preparation and control of Standard Operating Procedures and ensuring compliance with cGMP guidelines at all times.
  • Ensure compliance with current pharmacopoeias and all regulatory/company guidelines.


  • A third level Science Qualification
  • Minimum of 1-2 years pharmaceutical experience in a GMP regulated laboratory environment.
  • Strong oral and written communication skills. Ability to document, plan, market, and execute programs.

Fastnet has a strict confidentiality policy - please be assured that your details will never be forwarded to any third party without your consent.

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Glen Scheiner
Glen Scheiner
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