Scientist I - 1 year contract

• Working within a controlled ISO 13485 and ISO 9001 laboratory quality system and in accordance with GxP procedures. • Design, plan and execute Physical Testing in support of R&D activities and base business projects in accordance with applicable procedures and guidelines. • Development and validation of new Physical Testing methods. • Estimating the resources and time required to conduct an experiment and monitoring performance to ensure targets are met. • Author validation protocols, reports and technical documents for medical devices/pharmaceutical products. • Perform basic statistical analysis of test data. • Prepare and present internal presentations to present findings of the laboratory. • Effective organisation of assigned workload; ensures integrity of all data generated and timely/accurate provision of results to GLP standards. • Accurate recording and analysis of laboratory data in accordance with good documentation practices. • Perform detailed laboratory investigations to determine the root cause analysis of atypical and out of specification results, apply corrective and preventative actions and author concise investigation reports. • Assist in laboratory test method/procedural revisions. • Ensures laboratory compliance with cGMP regulations and SOP’s/TD’s. • Involvement in change control activities and associated actions. • Support laboratory daily activities such as laboratory housekeeping, equipment maintenance and calibration, solution preparation, consumable stock replenishment, shipping samples, scanning documentation, logging of samples etc.