Company: Cpl
Location: Dublin



Full-time, Contract

€36,000 a year

Quality Control Analyst – Graduate Opportunity

Cpl in partnership with our client Pfizer are currently recruiting for Quality Control Analyst in their Grangegorman site.

Job Responsibilities:

  • Perform analysis on finished drug product, in process materials and stability samples – UV, HPLC, wet chemistry.
  • 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 e.g. 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.
  • Ensure relevant assays are performed on samples in support of release test and stability test programs
  • Support any validation and qualification of test methods and processes
  • Facilitate laboratory investigations and support associated product investigation
  • Support Laboratory inspection and audits


To be successful in this role the following are prerequisites to application:

  • Third level Qualification in Science, Engineering or equivalent is preferred though not essential. Exceptions may be considered where relevant skills/experience and correct attitude and behaviors exist (this may be supplemented by further education in parallel)
  • 6+ months pharma experience
  • Excellent communication and interpersonal skills
  • This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of all activities, duties or responsibilities required of the incumbent. Incumbents may be asked to perform other duties as required

Job Types: Full-time, Contract

Salary: €36,000.00 /year


  • Pharma: 1 year (Preferred)