Our client a global biotech company based in Speke are looking for a Microbiologist to join their microbiology department and perform QC laboratory tests on in-process, intermediate and finished vaccine products.

This role is to start as soon as possible and to last for 3 months (possible longer). There is also a possibility of other opportunities arising from the position for the right candidate.

The role is paying between £13.11 – £18.89 dependant on experience.

****Please do not apply for this role unless you are available immediately/on a 1 weeks notice AND are able to commit to shift work ****

Working patterns will vary dependent on the area but will be a mix of:
Days (Monday - Thursday 8am - 4.45pm, Friday 8am - 1pm) paying between £13.11 - £14.20 per hour
Shift 1 - Days 2 on 2 off (hours depend on area) the rate will range from £16.00 - £17.32 per hour
Shift 2 - 2 days 2 nights, 2 on 2 off - £17.44 - 18.89 per hour.

Key Responsibilities:

• To perform accurate and reliable laboratory tests and generate results to cGMP standard by entering and authorising test data. Including the investigation of any invalid, OOS/OOT results within the GLIMS system, in accordance with current company requirements and SOPs
• To consult with QA and where required initiate Sentry investigations where deviations have occurred
• To ensure that the maintenance, qualification and calibration of laboratory equipment used is up to date and at the required GMP standards
• To use only approved and validated assay processes and reagents
• To participate in laboratory administration, including the complete and review of log books and PCS alarms generated progression of Change Controls, SOP reviews and closure of assigned Corrective/Preventative actions
• To participate in department housekeeping activities, such as cleaning, ordering and maintenance of stocks
• To participate in planning and execution of ad hoc projects such as technical and validation studies
• To troubleshoot in the resolution of testing problems where required
• To maintain responsibility for upkeep of training records

Key Skills/Experience:

• Experienced in the relevant testing discipline within the Pharmaceutical industry
• Experience of Quality Control testing techniques
• Experience in cGMP environment or Industry practices
• Awareness of test and equipment validation
• Knowledge of continuous improvement and root cause analysis techniques
• Educated to NVQ level 2 or equivalent in a relevant scientific discipline as a minimum requirement
• Computer Literate
• Bio-assay experience is essential