Microbiology Team Coordinator
Liverpool, UK
3h ago


  • To ensure appropriate standards of cGMP, housekeeping, Health, Safety and Environment are applied in the team, in accordance with current regulations and procedures guaranteeing that the area is permanently inspection ready.
  • To schedule the activities of the team in accordance with the Lean Lab solution, monitoring and approving holidays, sickness absence and training / competence position of all associates.

    The monitoring of associated KPIs being used to adapt plans accordingly. To review and approve data generated from testing and to bring to the attention of the Team Manager and other site personnel test results and any trends, out of specification results.

    In addition, where appropriate perform the required transactions to release materials. To ensure that the maintenance and qualification of the specified laboratory and equipment within is up to date and at the required GMP standards.

    To ensure the use only of approved and validated test processes. To co-ordinate department cGMP systems, such as deviation management, closure of corrective and preventative actions, change controls and SOPs.

    To participate in improvement project teams where required driving quality decisions and provide advice and technical support where required.

    Coordinate completion of any resulting activities. To lead troubleshoot in the resolution of testing problems involving your team and relevant customers / suppliers.

    Demonstrate creative problem solving within cGMP constraints and align with best practice. To track the team ensuring that mandatory training is in place.

    To encourage optimal performance of staff through training, feedback every two months and development planning in conjunction with the Team Manager Education Graduate level in relevant discipline or suitable alternative or equivalent experience within industry.

    Computer Literate. Capabilities cGMP background in the Pharmaceutical industry Experience of Quality Control testing techniques and industry practices. ements

  • Authors protocols and reports for suitability studies and investigations to support testing and compliance issues
  • Ensures laboratory instruments are qualified, calibrated and properly maintained and documentation complies with cGMP standards
  • Assists in development of new methods and procedures and maintains standard operating procedures (SOPs)
  • Documents quality issues and performance measures for management review Minimum 3 years working within a QC Laboratory
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