3 jobs found in Milton Keynes

Job summary We have an exciting opportunity for a Specialist Biomedical Scientist in Clinical Biochemistry/Immunology. The service supports all hospital wards and departments, as well as GPs, clinics, and private hospitals across central and south Buckinghamshire and beyond. The central laboratory is based at Stoke Mandeville Hospital, with a satellite laboratory at Wycombe Hospital. Staff are expected to work at either site as required by the service. Main duties of the job As a Specialist Biomedical Scientist in Clinical Biochemistry, you will be responsible for processing laboratory tests on patient samples across one of four sub-sections of the laboratory on a rotational basis. Applicants must hold HCPC registration as a Biomedical Scientist and possess strong knowledge in Clinical Biochemistry and Immunology. Ideally, you will also have experience in personnel management. The department is well-equipped with modern, standardised analysers, including Architect, Tosoh, Osmo 1...

Are you looking to earn excellent rates of pay equivallent to in excess of £54,000+ per annum? * 12 hour shift * 9am - 9pm * 4 days on, 4 days off * £21.74 - £25 per hour * Positions available to start from 28th April 2025 We have opportunities with immediate start available, pending compliance and employment checks, with a pharmacuetical business located in Coventry. Working from their facility you will join as part of an expanding multicultural team of Phamicists, ACT's, Dispencers and support staff. Key Responsibilities: * Accurately check and verify dispensed prescriptions in line with SOPs and legal standards * Ensure safe, timely preparation and dispatch of medications * Maintain accurate patient records (PMR) and uphold data protection standards * Identify and escalate medication-related issues to the Responsible Pharmacist * Support stock management, including ordering, receiving, and regular checks * Ensure proper storage of medicines and maintain a...

We are seeking a Process Technician to support production operations within a pharmaceutical GMP-regulated environment. This role involves operating and monitoring manufacturing equipment, maintaining batch documentation, and ensuring compliance with pharmaceutical quality, safety, and hygiene standards. Key Responsibilities * Operate and monitor production equipment in line with SOPs and GMP requirements. * Carry out raw material charging, equipment setup, cleaning, and basic maintenance. * Maintain accurate batch documentation and production records. * Identify and report process deviations and support resolution activities. * Support continuous improvement and updates to procedures where required. * shift work will be required Requirements * Experience in pharmaceutical, GMP, or manufacturing environments preferred. * Strong attention to detail and ability to follow procedures. * Good communication and teamwork skills