1 to 8 of 8 Regulatory Compliance Jobs in Wales

including managing electronic approval systems and ensuring timely reviews. Version Control: Implementing a robust version control and maintaining accurate versions of documents to ensure compliance with regulatory standards and facilitating updates as required. Quality Compliance: Ensuring documents meet quality standards, regulatory requirements, industry standards and Good … the development and implementation of training programs related to document control processes. Audit Support: Preparing and providing documentation for internal and external audits, ensuring compliance, and addressing audit findings. Electronic Document Management Systems (EDMS): Proficiency in utilizing EDMS for efficient document control and management. Like SAP, Veeva (VQD), COMOS..etc. … document-related processes and changes within the organization. Continuous Improvement: Identifying opportunities for process improvement within the document control system to enhance efficiency and compliance and adherence to best practices. Maintaining the integrity of documentation, ensuring that processes adhere to quality standards and regulatory guidelines. Requirements: High School more »

Manager to join our team, based at our site outside of Cardiff. As Quality Assurance Manager, you will play a pivotal role in ensuring compliance with quality standards, maintaining our quality management system, and driving continuous improvement in quality practices across the organisation. The role of Quality Assurance Manager … to our customers, meet consistent standards and adhere to quality requirements. Responsibilities will include: Overseeing all aspects of quality assurance for the site, ensuring compliance with regulatory requirements. Developing and maintaining an internal audit program covering regulatory compliance and quality assurance. Collaborating with cross-functional teams more »

looking for a Quality Systems Engineer to provide support to the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to … ensure compliance with necessary regulatory bodies in the areas of: Corrective and Preventive Action (CAPA), Complaint, Post Market Surveillance and Non-conformance Report (NCR). Provision of advice according to established procedures relating to CAPA, Complaint, Post Market Surveillance and NCR and against the external requirements of the … relevant regulatory authority (ISO13485, Medical Device Directive MDD 93/42/EEC/Medical Device Regulation (EU) 2017/745 and 21 CFR Part 820) and local quality standards. Provide effective solutions/advice to design and manufacturing teams on established procedures to ensure products are designed and more »

looking for a Quality Systems Engineer to provide support to the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to … ensure compliance with necessary regulatory bodies in the areas of: Corrective and Preventive Action (CAPA), Complaint, Post Market Surveillance and Non-conformance Report (NCR). Provision of advice according to established procedures relating to CAPA, Complaint, Post Market Surveillance and NCR and against the external requirements of the … relevant regulatory authority (ISO13485, Medical Device Directive MDD 93/42/EEC/Medical Device Regulation (EU) 2017/745 and 21 CFR Part 820) and local quality standards. Provide effective solutions/advice to design and manufacturing teams on established procedures to ensure products are designed and more »

looking for a Quality Systems Engineer to provide support to the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP)./p br Considering applying for this job Do not delay, scroll … possible to avoid missing out. br p The successful applicant will:/p ul li Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of.../li/ul br p JBLK1_UKTJ/p more »

Job summary The post holder will lead the provision of a high quality, safe and effective pharmacy clinical trials service, to ensure compliance with the required National Standards and UHBResearch and Development Strategy. The post holder will be the Pharmacy Lead Facilitator for Research and Audit projects. They will … will work closely with the Health Board's Research & Development department and, supported by our highly experienced Senior Pharmacy Trials Technician, will provide expert regulatory knowledge with regards to GCP and pharmaceutical aspects of clinical trial delivery and management. The ideal applicant will be a highly motivated and methodical … and that controlled drugs are securely managed. Support the Research and Development Department by producing reports on Medicines Management aspects of R&D, including regulatory compliance, financial and activity based data. Identify and review clinical treatment protocols and make appropriate changes and prepare drug protocols and briefing papers more »

Develop methods of analysis in order to deliver fully validated assays • Coordinate analytical studies from client onboarding to final reporting with accountability for the regulatory compliance and scientific integrity of the study. • Perform and supervise the processing of samples using Immunoassay techniques • Document procedures undertaken and apply QC more »

looking to expand the team as they are looking for a Document Specialist I. You would be responsible for reviewing Engineering test files for regulatory compliance and conducting related research. Responsibilities : Maintains an understanding of the certification compilation and research process, including methods for obtaining required information Review more »