Were 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.
Reporting into the Quality Control Manager, the Quality Control Specialist will ensure that objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to their customers.
The QC Analyst will perform and review a range of techniques such as immunoassays, cell based potency bioassays, HPLC and compendial methods as part of routine and non-routine testing and project work to ensure processes and end products comply with corporate and regulatory requirements to facilitate product release.
Duties: Work as directed by the QC Manager / Associate Director, according to Company safety policies, c GMP and c GLP.
Required to drive compliance with companys 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.
Required to comply with companys Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (c GMP) in the performance of day to day activities and all applicable job functions.
Develop, implement and maintain procedures that comply with appropriate regulatory requirements.
Ensure that all Quality Systems within the department are adhered to on a daily basis.
Operate as part of the QC team performing the allocated testing and laboratory-based duties.
Ensure timely completion of all assigned data processing and reviewing.
Ensure timely completion of Laboratory Investigation Reports and deviations through site procedures Participate in the timely generation of trend data, investigations, nonconformances, validation protocols, reports in support of method validation/verifications and equipment qualifications.
Participate in QC Tier 1 daily meetings and ensure effective communication of testing progress, deviations etc.
Peer review testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved.
Where applicable, review, approve and trend test results.
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.
Experience, knowledge and skills: 1-2 years of experience in a c GMP laboratory environments.
Bachelors degree or higher preferred; ideally a science related discipline Knowledge of regulatory/ code requirements to Irish, European and International Codes, Standards and Practices.
Knowledge of c GMP Laboratory Quality Systems Report, standards, policy writing skills required Understanding of Lean Six Sigma Methodology preferred.
Immunoassay and cell culture experience preferable If interested in this posting please feel free to contact Avishek Singh on or for further information.