Job Description
A diagnostics manufacturer has an exciting 12 Month Contract for a QA Officer to join the team. The main purpose of the role will be to ensure compliance within the Quality Management System (QMS). You must have previous experience in an ISO9001 compliant QA function.\n\nRESPONSIBILITIES\n\n•Work closely with the QA/RA Manager managing the Quality Management System.\n\n•Assist all quality and regulatory projects, processes, and activities \n\n•Reviewing and approval of QA-controlled documentation (such as SOPs, batch records, working instructions, non-conforming work);\n\n•Support for the development of appropriate Corrective and Preventative Actions (CAPAs) and continuous improvement activities.\n\n•Maintenance of training records matrices for relevant staff\n\n•To provide administrative support to the QA/RA department and any other duties as requested \n\n•Assist in regulatory audits i.e., ISO9001\n\n•Lead on internal audits\n\n•Act as point of contact for Manager for QA related tasks when QA/RA Manager is not on site\n\nQUALIFICATIONS\n\nEducated to A levels standard.\n\nDegree in Life Sciences (related subject) desirable but not essential\n\nAt least 2 years’ experience in a QA regulated environment, industry or science-based company desirable but training will be provided.\n\nUnderstanding and knowledge of Quality Management Systems (QMS)\n\nGood communication and interpersonal skills\n\nAbility to work proactively both individually and as part of a team\n\nStrong statistical data analysis skills\n\nAbility to be methodical, conscientious, organized and show attention to detail\n\nTo maintain a high level of integrity, motivation, and reliability in all work\n\nTo be decisive where needed, display decision making and problem-solving skills\n\nComputer literate\n\nAttention to detail\n\nTime management skills\n\nHybrid: 1-2 days from home after probation