Qc Analyst - Hplc - Biopharma - Athlone

Job DescriptionThe role will primarily involve supporting method development and optimization activities for finished product testing, transfer and validation according to regulatory guidelines and may include routine testing for example dissolution and HPLC testing.RequirementsA degree in Chemistry or a related discipline is requiredHPLC and dissolution experience is essentialMethod development and optimization experience is requiredA minimum of 2-3 years' experience in a GMP pharma environmentExperience with technical transfers and validation is desirableDemonstrate problem solving in delivering process and analytical understanding.Good understanding of requirements for working in a GMP environment.Good understanding of Empower 3 SoftwareAbility to quickly learn new processes.Ability to communicate clearly and to form strong working relationships with colleagues.Ability to work on own initiative and be capable of developing solutions to problemsWilling to operate in a flexible manner and be able to switch priorities at short notice.Good team player, organised, accurate, have strong documentation skills.Passionate about quality and customer service.Good communication skills both internally and externally.PackageCompetitive SalaryPermanent Full time positionBenefits include medical insurance, pension and life assurance.