QC Analyst

  • Cork
  • Temporary 12 months
  • JO-1906-64599_1561645426

Summary

The Quality Control Analyst will be responsible for testing and release activities for API raw materials, intermediates and finished products.

Responsibilities:

  • Responsibility for performing analysis on raw materials, intermediates and bulk drug substances in line with cGMP.
  • Performance of a range of analytical methods/assays including KF, UV, FTIR, GC & HPLC.
  • Calibration of laboratory instrumentation.
  • Conformance with Departmental SOP's.
  • Adherence to good laboratory practices and housekeeping standards.
  • Assistance in the creation and maintenance of laboratory procedures and associated documentation.
  • Review of analytical data for GMP compliance.
  • Data entry & review in the SAP system.
  • Support of laboratory investigations and corrective action tasks.
  • Sampling of raw materials.
  • Environmental and utilities sampling.
  • Other laboratory related tasks as required.

Required Skills:

  • Pharmaceutical experience in a GMP regulated laboratory environment.
  • Good communications skills.
  • Proven ability to work on own initiative.
  • PC skills MS Word, Excel etc.
  • Proven technical ability in laboratory systems.
  • HPLC & GC experience preferred but not essential

Qualifications Required:

  • BSc in a Scientific discipline.
  • 2-5+ years minimum work experience in the pharmaceutical or related industry.

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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