Manufacturing Operations Expert

1 month ago


Liverpool, Liverpool, United Kingdom CSL Full time

Job Summary

The Process Technician will be a key member of the manufacturing organization, responsible for operating and performing a broad range of varied work activities that support team objectives. The purpose of this role is to support the manufacture of viral seed stocks for use in the Influenza Vaccine manufacturing process.

Key Responsibilities

  • Ensure that all Departmental Standard Operating Procedures (SOPs) and Manufacturing Instructions (MIs) are followed and implemented correctly.
  • Ensure appropriate control, monitoring, and delivery of activities in their area of work, maintaining a high level of quality and efficiency.
  • Ensure that all documentation is completed correctly, accurately, and in a timely manner, and signed by the relevant personnel.
  • Carry out final documentation review and sign off to ensure documentation is accurate and complete.
  • Ensure compliance to Health and Safety regulations, consistently demonstrating behaviors necessary to create a safe working environment for themselves and their colleagues.
  • Be able to update existing SOPs and MIs as and when required, performing regular reviews and initiating new documentation as appropriate.
  • Actively maintain and promote a Current Good Manufacturing Practice (cGMP) compliant culture, ensuring that the highest standards of housekeeping and safety are applied within the area in accordance with regulatory requirements.
  • Maximize individual contribution to achieve team objectives, working as a team member, providing and receiving support, feedback, and communication with team members and their leader.
  • Attend all compulsory and allocated training courses required for the role, ensuring that all training is completed in a timely manner and personal training records are kept up to date.
  • Work in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines, and site procedures for Health, Safety, and Environment.
  • Contribute ideas and actions to improve team, process, and equipment performance, supporting process improvement and upholding Seqirus Values and Behaviors.
  • Support organization change and process improvements.

Experience Requirements

  • Experience in working in A/B Grade clean room environment operations.
  • Experience of aseptic manipulations and working in a controlled environment.
  • Skilled worker with relevant experience in pharmaceutical, biotechnology sterile production.
  • Knowledge of cGMP.
  • Mechanical aptitude and knowledge of electronic mechanical equipment.


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