Material QC Analyst

£27000 - £30000 per annum
  1. Permanent
London
  1. Technical Operations, Quality Control, Microbiologist
Posted: 09/06/2020
BBBH14225

This vacancy has now expired. Please see similar roles below...

Hobson Prior is currently working with a gene therapy organisation who are determined to develop possible curative treatments for patients who are living with serious illnesses. This pioneering company is seeking a Material GC Analyst to manage incoming materials and support Good Manufacturing Practice compliant activities for the QC release of product and incoming materials.


Job Responsibilities:

  • Complete inspection of incoming materials, following SOPs and GMP practices to ensure seamless supply of material to support aseptic manufacture of ATMP product.
  • Physical inspection of raw materials. Ensure the warehouse storage environment is acceptable for the materials being inspected (Can be multiple warehouse locations).
  • Monitor the material inspection programme ensuring materials are suitable for the manufacture of gene therapy products to the required standards.
  • Coordinate incoming material testing where required.
  • Maintain all incoming material documentation meets GMP requirements.
  • Ensure adequate control of the material status for release or Reject.
  • Comply with the organisation's procedures including Health and safety and GMP.
  • To ensure all equipment used is calibrated/maintained and in line with SOP's.
  • Recognise and report procedural problems and deviations.
  • Partake in the planning of duties to ensure the facility is acceptable and customers receive products on time and in full.
  • Identify and support method/technology improvement activities and facilitate implementation into the microbiology department.
  • Any other duties/projects within the skills and ability of the post holder.

Key Skills:

  • Proficiency in Microsoft Office software (Word, Excel and PowerPoint) preferred.
  • A high Level of attention to detail.
  • Looks for ways to improve and promote quality; demonstrates accuracy and thoroughness.
  • Prioritizes and plans work activities; uses time efficiently.

Requirements:

  • Minimum 1 years' experience working in a GxP environment.
  • Experience of quality documentation.
  • Experience of working within a GMP manufacturing environment.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

Upload CV