Overview LSC have a great contract opportunity for a Senior Specialist, QC Quality Systems to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.
If you have 3 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for youKey Responsibilities Lead and manage QC Investigations assigned Facilitate root cause analysis and problem solving sessions Complete the generation of associated investigation reports Determine and create CAPA's, Effectiveness Reviews, and Supplemental Tasks as required Present investigations at IRB to senior management Leading and coordinating the initiation, implementation, and closure of QC Change Controls Requirements / Qualifications Education minimum of a B.
Sc.
Biochemistry or related discipline At least 3 years' experience, in a GMP laboratory setting ideally within a biologics laboratory A minimum of 1 years' experience with demonstrated effectiveness using quality systems (investigations/change controls - Trackwise/Infinity) in a FDA and EMA regulated environment Knowledge of biologics QC testing (Separations, Bioanalytical, Microbiology, Raw Materials and Stability testing) is desirable Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1 G/Stamp 4 visa to applyApply via this advert or contact Siobhan Cummins on if you have any more questions about this role
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