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Clean Room Operator Full Time

at Fresenius Kabi Limited London in London (Published at 26-03-2022)

Overview:

Are you an organised and focused Operator, with a great depth of experience in Production or Packing Halls?


Due to business growth, we are looking to expand our Aseptic Services Unit. As a Clean Room Operator, you would be responsible for assembling batches in the assembly area per batch documentation and completing necessary paperwork in alignment with standard operating procedures.


This role will be 37.5 per hours a week Monday-Friday, 7am - 3pm alternating with 3pm - 11pm on a weekly basis and it will be based in Runcorn.
Fresenius Kabi is a global healthcare company that specializes in lifesaving medicines and technologies for infusion, transfusion and clinical nutrition. The company's products and services are used to help care for critically and chronically ill patients.
With a corporate philosophy of 'caring for life', the company's goal is to improve the patient's quality of life.
Our product portfolio included a comprehensive range of IV generic drugs, infusion therapies and clinical nutrition products as well as the medical devices for administering these products.
Responsibilities:
  • Assembling batches as per batch documentation, completing all necessary paperwork and transferring materials into the ASU

  • Reviewing post compound documentation to ensure that the product produced is to the required standard and labelling the product according to the defined procedure

  • Assembling raw materials for batches in accordance with the received batch documentation

  • Prepare the Bill of Materials (BOM) for the following days production

  • Working to a production plan to deliver batches to the compounding schedule

  • Maintaining production output through supporting continuous work flows

  • Ensuring all materials and components are replenished in preparation for start up on the next shift

  • Carrying out documentation duties required under good manufacturing practice

  • Ensuring areas are maintained and cleaned in accordance with ?good housekeeping? practise and standard operating procedures

  • Ensuring the appropriate disposal of waste from the grade C area is in accordance with current procedures
  • Involvement in process improvement e.g. Quality/Efficiency improvements

  • Recording and communicating any issues affecting quality or efficiency

Qualifications:
  • Aseptic or Pharmaceutical manufacturing experience ideal but not essential

  • Good communication skills to ensure active motivation and good team work

  • Good organisational and planning skills

  • Able to deal with stress and absorb pressures

  • IT literate and strong numerical skills

  • Trained in manual handling procedures and health & safety awareness

  • A good understanding of cGMP requirements


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