QC Analyst

Location: Haverhill, Suffolk Salary: £15.00 - £18.00 per hour
Sector: Pharmaceuticals Type: Contract
Contact: Matt Henocq Job Published: 8 days ago

QC Analyst

Responsible for analysis (sample/equipment), review and collation of experimental data against specifications laid down by the Quality department

Key responsibilities:

  • Sampling and analysis of raw materials, drug substances and drug products.
  • Ensure stabilty testing is initiated and completed within the required time frame.
  • Documenting analytical data and results according to cGMP.
  • Collation of analytical data into release packs and generation of C of A's as required.
  • Review of raw data, where appropriate, ensuring all documented results are in accordance with the appropriate product/material specification and good documentation practice.
  • Responsible for first line troubleshooting.
  • Cross value stream working to support the QC function.
  • Training and support of coleagues where appropriate.
  • Supports projects on an as required basis.
  • May be required to support equipment requalifications, calibrations, services etc.
  • Ensure that equipment is maintained and fit for purpose against site procedures before use.
  • Carry out Risk/COSHH assessments and ensure that the laboratory is maintained in a safe and tidy manner at all times.
  • Raise Events, CAPA's & Laboratory investigations immediately or within the required time frame from detection.
  • Complete all corrective and preventative actions within the agreed timelines.
  • Maintain core training and prior to conducting any activity ensure you are trained in the current version.
  • Responsible for personal safety and that of others, reporting all accidents and unsafe acts and conditions.
  • Ensure that the laboratory is maintained in a safe and tidy manner and record all cleaning activities according to cGMP.
  • Identify and implement improvements to ways of working with an aim to standardise each working week.
  • Take responsibility for adhering to cGMP requirements during all activities performed, and seek clarification of requirements when they are unclear.

Required skills and experience

  • Demonstrated ability to work consistently to quality policies and cGMP
  • Proven, sustained competence in analytical techniques and skills relevant to group
  • A working knowledge of laboratory health and safety
  • Demonstrated ability to successfully manage own workload to meet departmental targets
  • BSc Science related discipline (Chemistry/ Biochemistry preferred)

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