Senior QC Analyst

Job title:

Senior QC Analyst

Company

Cpl Group

Job description

On behalf of my client, a global pharmaceutical, we are collaborating with them on a new role for a Senior Analyst. This is a permanent role with a 2-cycle shift.Position SummaryReporting to your Area Supervisor, conduct analysis as scheduled/requested by your supervisor and by making the best possible use of available resources.Duties and ResponsibilitiesKey duties and responsibilities may include:Operational:

  • Conduct all tests, as instructed/scheduled by your area Supervisor, and in a timely manner.
  • Be aware of the daily, weekly, and monthly KPI targets, schedule adherence requirements and Service level agreements (if applicable) of the area and of the importance of consistently achieving applicable targets.
  • Assisting & performing (Leading) root cause problem solving exercises (e.g. 5 Why’s, Fish bone diagrams etc) as required.
  • Troubleshooting of equipment as required in the event of issues.
  • Host all Scheduling/Piloting Meetings in absence of Supervisor or as Designated.
  • Review, check and update relevant documentation as necessary e.g. SOP’s, standard work, Methods/Specifications etc.
  • Ensure all equipment in your area is within calibration. You are required to use and maintain it in the correct manner.
  • Exercise good housekeeping and GLP practices daily by acting as a role model to your colleagues in terms of attitude, actions, garbing, wearing of PPE etc.

· Work co-operatively and flexibly both within your department and with other departments.· Be prepared to undertake additional tasks as requested to meet operational or business requirements.· Contribute positively to the performance culture and effective operation of the laboratory.Position RequirementsEssential:· Degree in Chemistry/Analytical Science/ Pharmaceutical Scienceor Forensic Science· Strong IT skills· Strong attention to detail· Demonstrate strong use of initiative/self-motivation and a disciplined approach.· Good communication skills· Strong positive attitude is essential for this position.· Minimum of 3 Years Experience of working within a GMP Laboratory ideally within the Pharmaceutical or Biopharmaceutical Industry.For additional information and full job spec email your CV to or call Tina at +353 1 2784701. Thornshaw Scientific is a division of the CPL Group

Expected salary

Location

Wicklow

Job date

Fri, 12 Jul 2024 02:44:59 GMT

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