QC Chemistry Analyst

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Job Description


CPL in conjunction with our partner Pfizer have an multiple roles available for QC Chemistry Analysts within their Grange Castle Facility. The role is to maintain regulatory compliance through established programs for laboratory testing, maintenance, training, and SOPs within QC Chemistry.

Discription / Responsibilities: 
• Perform Chemical analysis on finished drug substance, drug product, in process materials and stability samples. 
• Responsible for calibration and use of laboratory instrumentation. 
• Complete documentation associated with analytical results in a timely manner. 
• Report and document any non-conformances to the QC Supervisor. 
• Assist in the preparation and review of area documentation (SOP’s, Reports, Protocols). 
• Assist in the training of other analysts. 
• Ensure training compliance within assigned work area and QC. 
• Perform and assist in additional duties as directed by the QC Supervisor. 

• Experience in High Performance Liquid Chromatography with Empower, Capillary Electrophoresis, Part Mat, Osmolality, pH, appearance testing, UV, Karl Fischer, SDS Coomassie. 
• Experience with Lab systems an advantage. (LIMs, CDAS, Trackwise, PDOCs) 
• A relevant third level qualification preferably with a minimum of 2 years previous laboratory work experience in a cGMP pharmaceutical environment. 

Contact me in confidence to discuss further. Eamonn 01 614 6069 - eamonn.errity@cpl.ie

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Eamonn Errity

Talent Partner +353 1 6146000 Eamonn.errity@cpl.ie
  • Salary:Negotiable
  • Location:West Dublin
  • Type:Contract
  • Category:Science
  • Ref.no:JO-1801-366211_64