Senior Technician Quality Control, Carlow

Senior Technician Quality Control
Shift
RK25920
Contract 11 months
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.



Key Responsibilities:

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 functionsParticipate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etcParticipate 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 sameOperate as part of the QC team performing the allocated testing and laboratory-based dutiesPerform 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 requirementsPeer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achievedParticipate in the laboratory aspects of OOS investigationsProvide 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 on site.


Education and Experience:
Bachelors Degree or higher preferred; ideally in Analytical Chemistry/ Biochemistry or a closely related discipline2- 3 years’ experience in a pharmaceutical laboratory, ideally with experience in HPLC and relevant systems and software. Core to the role is to perform testing of samples to support the release of our key drug products.Good working knowledge of HPLC systems and software is desirableGood knowledge of cGMP, GLP, Quality Management Systems


If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.