1 to 6 of 6 Permanent QMS Jobs in Hertfordshire

sites. In this role you will be key in the following areas… • Providing review and approval of validation lifecycle documents from a variety of QMS within the company. Provide meaningful comments to ensure compliance with regulatory expectations/requirements. • Provide quality oversight of internal business groups and external services partners more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

Systems (CDS), Laboratory Information Systems (LIS), Bioinformatics Software, Statistical Analysis Software, Image Analysis Software, Chemical Inventory Management Software, Lab Automation Software, Quality Management Software (QMS), Environmental Monitoring Software, Programmable Logic Controllers (PLCs), Distributed Control Systems (DCS), Supervisory Control and Data Acquisition (SCADA) systems, Human-Machine Interfaces (HMIs), Industrial Control Systems more »

join the company. Permanent role with a competitive starting salary and extensive benefits package. Job Overview: Maintenance and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare more »

ISO 13485, UK MDR 2002, MDR 2017/745, MDD 93/42/EEC, MDSAP, and other related legislation. Prepare and maintain necessary QMS and regulatory documentation across the Group. Facilitate regulatory improvement initiatives CAPA Investigations: Conduct investigations and review customer complaints for vigilance. Key Tasks: Maintain compliant processes more »

compliance with ISO 13485, UK MDR 2002, MDR 2017/745, MDD 93/42/EEC, MDSAP, and other regulations. Prepare and maintain QMS and regulatory documentation. Assist QA Admin team with product approvals for UK and international markets. Evaluate suppliers and conduct approval audits. Document quality audits to … in a production/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 more »