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QC Analyst - 24/7

Contract Type: Permanent
Location: Dublin
Contact Name: John Reid
Contact Email: johnr@rftgroup.ie

Job Description

QC Analyst – 24/7

My client a leading Pharmaceutical company now requires a QC Analyst to join their expanding and busy laboratory.

The QC Analyst will have experience of Good Manufacturing Practice, current FDA & EMEA regulations for solid oral dosage pharmaceuticals for human use and a good working knowledge of manufacturing processes, packaging processes and validation activities used in the pharmaceutical industry.

This is a permanent role based in Dublin, it is a shift role for which a good shift premium will be paid.

Responsibilities of QC Analyst – 24/7
 
  • To observe GLP/cGMP at all times
  • Testing of all laboratory samples including Raw Materials, Packaging Components, Product, Validation, Stability, Environmental, OH
  • Performance of laboratory tests as per written procedure or as per pharmacopoeia
  • Recording of analytical results accurately
  • Operation, maintenance and calibration of laboratory instruments
  • Preparation and execution of instrument and method validation protocols
  • To maintain written training records
  • To ensure that the laboratory is kept clean, tidy and safe at all times
  • To report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior
  • Ordering, receiving and controlling laboratory chemicals, reagents and consumables.
  • Receiving and controlling test samples.

Requirements of QC Analyst
  • BSc. (minimum) in science or a related discipline.
  • Must have practical experience of HPLC, GC and Kf analysis.
  • Must have relevant experience in the pharmaceutical or related industry.
  • Must have a minimum of 18 Months experience in an analytical lab.
  • Must be available for shift work

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The RFT Group, BioPharmaceutical Division specialize exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.