Job Description
All work must be performed in accordance with current Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOP).
Responsibilities:
- Working in GMP Graded environments, including Grade D, C and B and the use of Grade A Restricted Access Barrier Systems
- Chemical sterilisation of antigens
- Vessel cleaning, sterilization and operation
- Set up and use of blending equipment and filling machine
- Equipment cleaning and preparation for autoclaving
- Defined routine maintenance and troubleshooting
- Accurate record keeping and documentation
- General housekeeping and cleaning of the production areas
- Completion of deviation investigations
- Performing periodic reviews of standard operating procedures
- Ownership of simple changes or tasks within the GMP change control and Corrective and Preventative Actions procedures
- Input into department schedule
- On the job training demonstrations for new operators
- Participation in daily dcepartmental planning meetings
- Completion of production SAP tasks for electronic record keeping
- Environmental monitoring and use of Laboratory Information Management System
The majority of the work will be with a team but occasionally you will need to work on your own.
Closing date for applications: 3rd December 2024
Current Contingent Workers apply
Not Applicable
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