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QC Chemistry Analyst

  1. Midlands (Ireland)
  1. Contract
Competitive
  1. CAPEX Projects
21-02-2024
33164
QC Chemistry Analyst - Pharmaceuticals - Carlow, Ireland - 11-Month Contract

Do you want to be involved with exciting Pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a QC Chemistry Analyst.

This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.

Role Summary:
  • Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP. Required to drive compliance with Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions.
  • Participate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etc.
  • Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same
  • Operate as part of the QC team performing the allocated testing and laboratory-based duties.
  • Perform various analytical techniques including but not limited to HPLC, (HIC, CE, IEX, HP-SEC), Capillary Electrophoresis and other compendial test methods in compliance with GMP requirements.
  • Peer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved.
  • Participate in the laboratory aspects of OOS investigations.
  • Provide support with audit/inspection requirements to ensure department compliance/readiness.
  • Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility.
  • Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g., FMEA, Fishbone diagrams, 5 why's etc,
  • Work collaboratively to drive a safe and compliant culture in Carlow.
  • 2 cycle shift Morning (7am -3pm Mom-Thu , 7am-2pm Friday ), Evening (3PM-11PM Mom-Thu, 2pm-9pm Fri)

Experience, Knowledge & Skills:
  • 2-3 years of experience in a pharmaceutical laboratory
  • A good working knowledge of HPLC systems and software is desirable
  • A good knowledge of cGMP, GLP, Quality Management Systems

If this role is of interest to you, please apply now!
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