staff on quality protocols. Responsibilities: Develop and improve quality assurance policies and procedures to ensure compliance with regulatory requirements and industry standards (e.g. BRC, GMP) Conduct regular audits and inspections of laboratory and manufacturing processes, equipment, and documentation to identify areas for improvement. Gain expert knowledge of the business management more »
degree level or above in life sciences, chemistry or a related file with experience of working in a regulated laboratory environment (e.g. GLP or GMP) • Experience in using and troubleshooting ELISA analytical systems as well as the ability to develop and validate analytical methods using ELISA. • The ability to document more »
safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift ... more »
development. Work with the project and business development managers from receipt of RFPS to develop firm proposals and subsequent project delivery. Ensure current GoodManufacturingPractice (cGMP) compliance. Maintain a safe working environment compliant with all relevant Environment, Health and Safety (EHS) requirements. Maintain and expand the cGMP QC services … and product specifications, Certificates of testing, Stability Study Protocols, Method Qualification Protocols and Reports. Manage the ongoing environmental monitoring and water testing of the GMP facility and operation. Manage the investigation of out-of-trend (OOT), out-of-specification (OOS) and any deviation events. Ensure that all regulatory expectations are … met regarding any GMP QC samples or data collected, manipulated, reported, stored or archived. Provide timely and accurate testing updates for materials, samples, products and stability studies to internal parties and external clients. Has budgetary responsibility for the QC department including management of spend and equipment capital expenditure ensuring development more »
safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position: Carry out Daily/weekly GMP audits as required. To complete a detailed shift report at the end of every shift. To audit daily process documents including monitoring weights on line more »
