1 to 21 of 21 CAPA Jobs in the UK excluding London

Healthcare. For successful applicants, Polar Speed will process basic disclosure criminal record checks. Key responsibilities: Actively support quality processes such as non-conformance and CAPA 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 and CAPA 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 »

tool for improvement as well as compliance and challenges existing practice where appropriate. Supports and process NC and/or Corrective and Preventive Action (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 CAPA and NC for medical devices A practical working knowledge of implementation of change control, and of all aspects of the process and equipment 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 »

projects Desirable but not essential skills to have would be: RCA (Root cause analyses techniques) Previous experience in a Pharma environment Exposure to QMS - CAPA's, CC, RCA etc Experience on all mainstream software packages including but not limited to Siemens, Allen Bradley and Mitsubishi. Medium to High manufacturing environment more »

Key responsibilities: Responsible Person and Responsible Person for Import Actively assist in the implementation and maintenance of quality processes such as non-conformance and CAPA management, change controls and risk assessments, and ensure that the quality system is continuously improved with the objective of assuring GDP compliance Provide support for … are maintained, and seasonal mapping and calibration activities are conducted in a timely manner Host and participate in regulatory and client audits and prepare CAPA plans addressing any observations identified Key Skills/Experience/Requirements: Successful candidate MUST be eligible to become a Responsible Person for Import. Exceptional knowledge more »

and Regulatory requirements and to ensure that proprietary information is protected at all times. Responsible for the recording and investigation of Non conformances and CAPA using root cause analysis tools where appropriate and regular reporting on NCs and CAPAs. Responsible for NC and CAPA 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 and CAPA, 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 »

requirements. Work Closely with Mixing and Production in the development of IPC's for new products. Support all site functions with technical investigations and CAPA 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 working to support and track actions that are to be taken. Support quality related investigations, assist in the development and approval of effective CAPA in order to resolve product, audit and customer issues. Support effective pre-audit preparation and post audit follow up of customer audits and regulatory inspections. more »

To conduct investigations to assess the probable root cause of any deficiency noted during process confirmation activities, informing the accountable function, and ensuring corrective and preventive action is taken./li/ul p Required Skillset:/p p To succeed in this position, you must have the ability to more »

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 »

the work Ensure that the products and services we deliver for our clients conform to the specified requirements and agreed standards Advise suitable corrective and preventive action following the identification of any quality issues Represent as required for customer meetings ensuring customers and companys quality standards are understood and implemented more »

Job Posting Title: Quality Manager - Level 3 Site: Hertfordshire SG12 0DP Duration: 6 months Onsite Hours per Day 7.5 Hours per Week 37.5 due to mat cover broad ranging QA role - need experience in QA docs for blenders, chillers, chill more »

attend study days and training programs as requested by Senior Technician, ASU to ensure continuing personal development. To highlight potential corrective and preventable actions (CAPA) and service improvements to enable colleagues to learn from errors or quality issues. To undertake any other related duties as may be deemed necessary. To … within an aseptic unit Experience of creating debtor forms, dealing with invoice queries. Experience of conducting risk assessments and COSHH assessments Experience of implementing CAPA Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary more »

Production Records and Quality Control testing data. Non-conformance:Coordinate and approve/manage to completion any non-conformances, deviations and out of specifications. CAPA:Coordinate and approve/manage to completion any CAPA raised. Ensure adequate root cause analysis has been conducted and any corrections or corrective/preventative more »

milestones and deliverables effectively and report and communicate progress to stakeholders. Report and investigate all incidents and adverse events entering the information in the CAPA module of Q-pulse in a timely manner, conducting Root Cause analysis and remedial action as required. Chair/lead and/or participate in more »

control audits and recording through approved channels as required. Report all incidents and adverse events to senior staff and enter the information in the CAPA module of Q-pulse in a timely manner as directed by senior staff. Demonstrate on going competency against training plans. Report all incidents and adverse more »

defined and applied within the business. • Coordination and leadership of reported quality/technical issues from business teams and customers, ensuring that appropriate corrective and preventive action is taken by the accountable function through use of multifunctional team activities and that the originator of the issue is informed. • To perform … To conduct investigations to assess the probable root cause of any deficiency noted during process confirmation activities, informing the accountable function, and ensuring corrective and preventive action is taken. • Compile and Present Quality overview to the leadership team within the business area Required Skillset: • Ability to interpret drawings. • Ability to more »

customer, regulatory, internal & compliance audits. Analysis of quality data & generation of quality reports. Support final product disposition & control of non-conforming material. Support the CAPA process, including deviations & customer compliant investigations, ensuring robust root cause analysis & appropriate corrective actions are implemented. Coaching and training of production and technical personnel on more »

quality audits to meet ISO, UK, European and worldwide regulatory requirements. Facilitate quality improvement initiatives. Analyse data for management reviews and non-conformances. Conduct CAPA and non-conformance investigations. Review customer complaints and maintain incident reporting. Meet LSAS objectives and targets. Core Competencies: Experience with BS EN ISO 13485 and … manufacturing environment. Internal and external quality auditing experience to ISO 13485. Passion for quality excellence. Previous quality assurance experience, including QMS documentation. Knowledge of CAPA and root cause analysis tools. Practical problem-solving approach. Understanding of ISO 14971 quality risk management principles. Self-motivated and team-oriented. Ability to manage more »

findings, and support supplier audits. Update Quality reports and KPIs. Analyze data for quality issues and support improvement initiatives. Initiate Corrective and Preventive Actions (CAPA) and Engineering Request Notes (ERN). Participate in ISO 9001, ISO 14001, and ISO 45001 internal audits. Attend Materials Review Boards (MRB) and process MRB more »