Process Operator

Responsibilities: P.O. generation and ordering for manufacturing to support production batches Assist with writing SOPs and Forms. Record data and log activities according to cGMP standards. Calibration, set-up and use of production equipment including - autoclave, balances, pH and conductivity meters, osmometers, Blood Gas Analyzers and peristaltic pumps. Prepare solutions, including buffers, reagents, and cell culture media and related tasks including but not limited to pH titration, osmolality adjustment, sterile filtration techniques, and sampling. Prepare and operate equipment according to written procedures (SOPs) Assist with setting up the GMP areas for batch production including received materials, stock counts and performing cleaning tasks. Sanitization of the WFI loop Perform routine WFI sampling for Production. Log production samples to QC. Requirements: Leaving Cert or equivalent. Higher Certificates or Bachelor's degrees in science-related fields desirable. Experience in GMP environment. Computer skills and familiar with MS Office. Randstad encourage applications from individuals of all ages & backgrounds. Whilst appointments will be made on merit alone candidates must be able to prove their right to work in the UK or the Republic of Ireland (as relevant). Randstad acts as an employment agency for permanent recruitment & an employment business for temporary recruitment as defined by the Conduct of Employment Agencies & Employment Business Regulations 2003 Skills: quality GMP pharmaceuticals production