Method Development & Validation SpecialistEurofins Food Testing Ireland LimitedRef: #JOB-2411505Application DetailsIn order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit. Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.Job DescriptionThe primary purpose of this role will be to develop and optimise analytical methods along with method validation and transfer according to regulatory guidelines. The role will involve participating in a Professional Scientific Services (PSS) team to ensure the highest quality and productivity standards are met along with the agreed client requirements and timelines.ResponsibilitiesComplete analytical data collection, interpretation and characterization of compounds while ensuring proper documentation of experimental data is adhered to.Support innovative development of new analytical methods as well as improvement and optimization of current methods.Provide technical expertise and analytical support for the introduction of new products to the Cork site, including method development, validation/qualification and transfer of methods to clients as required.Lead in troubleshooting analytical technical challenges during the development, validation/qualification and transfer of methods.Communicate regularly with client, providing updates on projects progress, addressing technical queries and delivering client project requirements to the defined timelines.Ensure the delivery of projects in the required timeframe and ensure that the site’s technical, quality and safety metrics are all achieved.Provide suitable training where required to adopt new practices.Review and approve standard operating procedures (SOPs), laboratory methods, COSHH assessments, laboratory investigational reports, validation protocols, risk assessments, reports & protocols.Accountable for adopting the ALCOA+ (attributable, legible, contemporaneous, original & accurate) principles and ensuring team working in accordance with registered methods and current Good Manufacturing Practice.Take a lead role in approval processes. Verify the quality and accuracy of analytical results and determine if material meets pre-defined acceptance criteria as per relevant SOPs, customer acceptance criteria, methodology, protocol and product specifications.Act as an analytical expert who provides expertise in laboratory practices and good manufacturing practices (GMP). Use this knowledge and experience to lead laboratory investigations or project/equipment design.Identify out of specification results, design root cause experiments and retest plans, ensuring investigations are completed in a timely manner with sound scientific rationale.Work on long-term objectives to deliver specific improvements or embed changes within the laboratory. Take ownership of projects from concept to delivery, providing progress updates throughout the lifetime of the project.Responsible for the scientific conduct of projects and communication of regulatory issues with senior level team members.Career LevelExperienced (Non-Managerial)
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