compliant manner. Ensure compliance with all Documented Quality system, FDA QSR’s and ISO 13485 requirements during day to day and assigned audit/CAPA activities. Maintain a good level of housekeeping in designated areas and observe all Health and Safety at work requirements. Operate within the company’s standard More ❯
Europe computer systems (e.g. SAP, Innova) and how they could best be utilised by the technical function. Participate in the investigation and documentation of CAPA plans to non-conformities found internally, secondary or Third Party audits. Liaise with customers/third parties for any issues relating to technical systems. Be More ❯
To perform out of specification/out of trend investigations To perform deviation/complaint investigations Assisting in the follow up of events andCAPA's To ensure correct QC samples are taken and sent for UK release testing in a timely manner The Person Minimum degree in pharmacy, biomedical … sciences, or any other scientific degree. 2 years' experience in a GMP/GLP role. Experience in CAPA, OOs, OOt, deviations, change controls etc in a GMP setting Willingness to learn. Strong administrative skills and the ability to generate clear and concise communication across all departments. Ability to prioritize work More ❯
