Job Description
QC Chemistry Analyst (Shift)RK2068311 Months Location: Carlow We're currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow.
This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties: Work as directed by the Quality Control Manager according to Company safety policies, c GMP and c GLP.
Drive compliance with Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (c GMP) 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 ensure 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.).
Education and Experience: Bachelor's Degree or higher preferred; ideally in Analytical Chemistry/Biochemistry or a closely related discipline.2-3 years of experience in a pharmaceutical laboratory.
A good working knowledge of HPLC systems and software is desirable.
A good knowledge of c GMP, GLP, and Quality Management Systems.
If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or rachel.kent@lifescience.ie for further information.
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