34 jobs
Russell Taylor Group Swadlincote £30,000 – £34,000 pa
Supports site validation activities across cleaning, computerised systems, equipment/utilities qualification and process validation, authoring protocols and reports and interpreting data against acceptance criteria. Works cross-functionally to maintain validated status of systems and processes, investigates non-conformances and supports regulatory inspections and internal audits.
SRG Lancashire
Maintains and improves a medical device Quality Management System in line with ISO 13485 and FDA QSR, leading non-conformance, deviation, complaint and CAPA investigations with root cause analysis. Supports internal, supplier and regulatory audits, risk management under ISO 14971, validation and design transfer, working with Manufacturing, R&D, Regulatory Affairs and Supply Chain.
Stryker Belfast £12 – £21 ph
Performs visual, dimensional and electrical inspection of sub-assemblies and final medical device assemblies, interpreting prints, drawings and wire lists to approve or reject in-process and final product. Also handles document review and archiving of DHRs, non-conformance quarantine documentation, ERP release transactions and First Article Inspection verification. Night shift role within a GMP-regulated quality team supporting KPI and throughput goals.
Oxford Nanopore Technologies Oxford
Join the Sequencing Development Team as a Development Scientist, contributing to the development and improvement of sequencing technologies. The role suits a highly motivated individual working within a dedicated scientific team in Oxford.
