MSAT Technician - Pharmaceutical - Cambridge - Contract Our client is a leading pharmaceutical manufacturer. At present, they are seeking an MSAT Technician on a temporary contract basis for 4 months at their facility in Cambridge. Overview: * Day to day activities in a sterile manufacturing facility, filling of sterile products, autoclaving and washing of components. * Maintaining the facility to GMP standards of cleanliness and environmental standards. * Ensuring all paperwork is completed to GMP standards and non-conformity documentation and investigation Key Responsibilities: * Ensure compliance with all regulatory requirements and maintain excellent GMP, quality control and safety. * Excellent attention to detail and accuracy, all paperwork to be completed accurately and in a timely manner compliant with cGMP. * Support the sterile Team Leader at weekly meeting, KPI’s, planning and deviation investigations * Experienced in working in a sterile environment, an isolator or RABS unit (Grade A). * Work with single use sterile technologies, and closed systems * Demonstrate ability to build bonds and work with other departments QA, QC, Validation etc. * Prepare autoclave and washer loads in accordance to procedure * Write and review new SOP’s and Batch records and roll these out to the team * Have the flexibility to operate in all areas of production, sterile operation, validation equipment, cleaning and autoclaving * On-going cleaning, environmental monitor and building compliance * Investigate any deviations and action CAPA’s * Perform regular cleaning of the cleanroom to ensure it remains within GMP standards. * Perform stock management tasks within the warehouse. Candidates will ideally have GMP experience in a production environment with experience of sterile production and demonstrated aseptic techniques. Additional skills: * Experience in GMP manufacturing. * Experienced in Clean Room Grade A environments, Isolators or RABS. * Should be assessor or qualified in safety systems, i.e. COSHH, risk assessments, manual handling or IOSH Managing Safely. * Experienced working with Excel and Word. * Knowledge of lean production or six Sigma. * Evidence of excellent attention to detail and ability to follow Standard Operating Procedures. * Experienced in writing SOPs for cleanroom activities. * Knowledge of validation operations, such as; FATs, SATs and IOQ/PQ