Warrington / Runcorn. Commutable from Liverpool, Chester, Manchester

Salary - Up to £45,000

Creative Resourcing, a specialist recruiter working within the manufacturing sector are currently seeking Lab Systems Analyst to work for one of our prestigious pharmaceutical clients.

Purpose of the Job:

To manage quality control (QC) and New Product Development laboratory system implementation, maintenance and use for the main manufacturing site (primarily and other UK sites where required) in accordance with site operations, quality & IS strategies and project plans.

Key Results areas are:

  • To act as the site expert on all laboratory computer systems - LIMS, CDS, standard-alone computer driven instrumentation and other applications identified by laboratory management. To develop and support appropriate administration and master data maintenance processes and procedures to ensure efficient day-to-day laboratory system operation.
  • To develop, maintain and deliver appropriate training modules for laboratory systems. Act as a key site expert of laboratory processes to ensure the appropriate knowledge is fed into IS laboratory system implementations.
  • To manage the implementation of the projects identified from the Runcorn site IS strategy which indirectly affects site laboratories. Liase with laboratory management and laboratory staff to gather information and translate into realistic IS system requirements.
  • Ensure new ways of working and lean practices are considered and employed during project implementations. Ensure that comprehensive and realistic training needs and requirements are defined and rolled-out for each project.
  • Ensure identification of new or modified business roles from IS systems implementation/upgrade. Ensure project controls are employed: risk and issue management, scope management, budget setting and control of expenditure within agreed levels.
  • Ensure appropriate service levels are developed and monitored for support of laboratory IS systems.
  • To ensure sufficient consideration is paid to all regulatory requirements for system implementation and maintenance including cGMP, computer systems validation, SOX, security and risk.
  • Assist in the generation and execution of validation deliverables.

Applicants should have the following experience/qualifications:

  • Graduate qualification
  • Experience working in or along-side laboratory operations.
  • Experience in working in a highly regulated industry, preferably Pharmaceuticals.
  • Project Management qualification preferable.
  • Familiarisation with Lean/process improvement concepts preferable.
  • Knowledge In depth knowledge of a wide range of laboratory systems gained from involvement in a significant systems implementation or upgrade.
  • Practical knowledge and experience in laboratory processes.
  • Working in a multi-disciplined team.
  • Commercial awareness and understanding of the operational and financial implications of decisions taken.


Our client is offering a salary of up to £45,000

This is a permanent opportunity to join a successful and progressive company that continues to enjoy market leader status. This vacancy is being advertised on behalf of Creative Resourcing who are operating as an employment agency.

Please only apply for this position if you possess all the necessary qualifications.

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Tuesday the 19th.

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