maintained Leads Internal audit program is performed as per the Internal Audit Program and presents findings during daily and weekly meetings. Follow up on CAPA's to ensure closure Maintain and improve quality systems by continuous improvement of HACCP/Preventive Control Plans and Food Safety and Quality programs against more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
allocate budgets, staff, tools, and specialized support necessary for efficient operations. Provide validation program leadership for Cepheid facilities, manufacturing processes and equipment. Maintain the CAPAand NCR systems, Calibration Program, Document Control and Lead site Change Management and Risk Management activities. Collaborate across the organization at all levels, across functional more »
tool for improvement as well as compliance and challenges existing practice where appropriate. Supports and process NC and/or CorrectiveandPreventiveAction (CAPA) to address operational issues within the PPA areas. Supports with project related document and technical review. Generation and monitoring of data streams and analysis to … functional teams whilst ensuring that deadlines are met. Competent auditor. Experience in hosting or acting as SME during external regulatory audits. Strong knowledge and experience of CAPAand NC for medical devices A practical working knowledge of implementation of change control, and of all aspects of the process and equipment more »
Healthcare. For successful applicants, Polar Speed will process basic disclosure criminal record checks. Key responsibilities: Actively support quality processes such as non-conformance andCAPA management, change controls and risk assessments, and ensure that quality system is continuously improved with the objective of assuring GDP compliance. Oversee the warehouse and … returns and exceptions are correctly processed in a timely manner. Participate in regulatory and client audits, lead internal audits/self-inspections and prepare CAPA plans addressing any observations identified. Investigation and reporting of incidents, including deviations, non-conformances, client feedback and customer complaints, including the logging, notification, investigation, reporting more »
internal/3rd party audit methods Experience of managing quality issues across a multi-site organisation Demonstrable experience in resolution of customer complaints andCAPA Experience in conducting audit and managing audit schedules (internal and third party) Demonstrable experience in writing policies and procedures and managing document control systems Experience more »
Bristol, Avon, South West, United Kingdom Hybrid / WFH Options
Smartbox Assistive Technology
Compliance and Quality Assurance Manager Our trailblazing global AAC (Augmentative and Alternative Communication) company, is on the lookout for an exceptional Compliance and Quality Assurance Manager to join our product development team and report to the Head of Hardware. At more »
requirements. Work Closely with Mixing and Production in the development of IPC's for new products. Support all site functions with technical investigations andCAPA actions linked to process/formulation non-conformances. Required Experience Qualified to at least BSc or equivalent in Chemistry or a similar technical discipline Good more »
and Regulatory requirements and to ensure that proprietary information is protected at all times. Responsible for the recording and investigation of Non conformances andCAPA using root cause analysis tools where appropriate and regular reporting on NCs and CAPAs. Responsible for NC andCAPA process management and regular reporting of … RA Manager & RP in ensuring that a quality management system (QMS) is implemented and maintained including quality risk management, documentation management, non-conformance andCAPA, change management, deviation processes, internal and supplier approval and audits as well as measurement of performance indicators and management review Take ownership for assigned projects more »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: CorrectiveandPreventiveAction (CAPA), Complaint, Post Market Surveillance and Non-conformance Report (NCR). Provision of advice according to established procedures relating to CAPA, Complaint, Post Market Surveillance andmore »
Hull, North Humberside, North East, United Kingdom
Umbilical Ltd
Participate in the review and approval of GMP documentation, including batch records, SOPs, and change controls. Assist in deviation investigations, root cause analysis, andCAPA activities to address quality issues. Aid in handling customer complaints, conducting investigations, and implementing preventive measures. Support in preparing for regulatory inspections and customer audits. more »
with cross-functional teams to investigate and resolve process and product quality issues deploying appropriate tools to assist root cause analysis. Conduct and facilitate CAPA, NC and complaint activities. Participate in facility internal audit programme and the hosting of external audits. Work towards departmental and facility objectives. Support the supplier … eQMS. Essential Skills & Experience Relevant engineering or science degree and/or relevant experience. Strong understanding of quality assurance and manufacturing processes. Experience in CAPA, NC, complaint and change control activities. Experience in highly regulated environment (healthcare, aerospace, defence). Experience of developing and auditing quality processes, documents, plans etc. more »
