QC Analyst

2 weeks ago


Middlesbrough, United Kingdom in Tenerife Full time

Middlesbrough, North East, United Kingdom

CK Group

30.04.2024

Full Job Description

QC Analyst

CK Group are recruitingfor a QC Analyst to join a leading pharmaceutical and chemicals CDMO,based at their site near Middlesbrough on a permanent basis.

Your main responsibility will include testing intermediates, productsand raw materials in line with demand and business requirements. 

Job Summary:

  • Follow approved methods andprocedures in accordance with cGLP & GMP requirements.
  • Report analytical results accurately and in a timely manner asdictated by internal and external customer requirements.
  • Ensure QC documents are complete, accurate and compliant withprocedures or guidelines.
  • Ensure that investigations areperformed in timely manner in accordance with set procedures. 
  • Carry out minor analytical method development to improveanalysis, including HPLC, GC, spectrophotometric techniques andtitrations.
  • Identify ways to improve reduction inturnaround times and reduce costs, whilst still adhering to corporatequality standards.
  • Assist in coaching and developing othermembers of the team.
Full Job Description

QC Analyst

CK Group are recruitingfor a QC Analyst to join a leading pharmaceutical and chemicals CDMO,based at their site near Middlesbrough on a permanent basis.

Your main responsibility will include testing intermediates, productsand raw materials in line with demand and business requirements. 

Job Summary:

  • Follow approved methods andprocedures in accordance with cGLP & GMP requirements.
  • Report analytical results accurately and in a timely manner asdictated by internal and external customer requirements.
  • Ensure QC documents are complete, accurate and compliant withprocedures or guidelines.
  • Ensure that investigations areperformed in timely manner in accordance with set procedures. 
  • Carry out minor analytical method development to improveanalysis, including HPLC, GC, spectrophotometric techniques andtitrations.
  • Identify ways to improve reduction inturnaround times and reduce costs, whilst still adhering to corporatequality standards.
  • Assist in coaching and developing othermembers of the team.
You will have the followingexperience/qualifications:
  • Chemistry (or very closelyaligned subject) degree with experience as an analyst in a finechemical or pharmaceutical industry role. HPLC and GC experience.
  • Experience of working in a GMP environment / methoddevelopment experience / cleaning validation experience.
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