8 of 8 QMS Jobs in the North of England

Job Title: Senior QA Specialist Salary: £38,000 - £45,000 Location: Greater Manchester SRG is currently working exclusively with a highly successful & award winning, CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all More ❯

Regulatory Affairs Specialist to join their QA/RA team on a 12-month maternity cover contract. Key Responsibilities: Lead and support continuous improvements within the Quality Management System (QMS) Collaborate with all departments and external stakeholders to maintain regulatory compliance Provide QA/RA expertise throughout product development and change control processes Guide risk management and post-market surveillance … Review SOPs, software development documents, and regulatory submissions Deliver training to ensure quality and regulatory understanding across the business Perform internal and supplier audits and support external inspections Validate QMS-related software and manage eQMS platforms Assist in compiling and maintaining technical and regulatory documentation Benefits At Genedrive, youll be part of a passionate and expert team, making a tangible More ❯

internal processes and procedures and external customer and regulatory requirements.• Maintain a clean, organised and safe working environment and organise 5S initiatives. • To ensure adherence to the group Quality Management System and compliance to all Customer and regulatory requirements including EASA Part 21, EN 9100 and NADCAP. • To prepare for and contribute to external audits with Customers and regulatory bodies. More ❯

a fantastic benefits package dependant on your experience. Hours are Monday - Friday, 37.5 hours a week. What will I be doing day to day? Responsible maintaining a documented Quality Management System, which reflects the site's commitment to Food Safety Legality and Quality and satisfies third party requirements. Ensure that the system satisfies the requirements of the FDA/FSMP … timely corrective action is taken when necessary. Responsible for the successful preparation and completion of all external and internal audits as well as responsible for presenting any documentation related QMS in all external audits such as SMAR Responsible for the co-ordination between the Environmental Management System and the Quality System to ensure adherence to GB and annex 4 standards. More ❯

Diagrams. Good fundamental electrical knowledge and ability to understand/interpret system drawings. Sound grasp of general IT/OT Technologies and development methodologies. Awareness/understanding of Quality Management System procedures. Knowledge of Windows Operating System configuration and lockdown. Knowledge of network switch and firewall configuration and network management packages. Electrical & Electronic or Electrical or Software Engineering degree (min More ❯

Job title: HCPC Clinical Scientist Reports to: Head of Laboratory Location: Based onsite at Manchester Science Park Contract Type: Full-time, Permanent Salary & Benefits: Competitive Salary + Benefits Package About Yourgene Health: Yourgene Health is a leading integrated technologies and More ❯

all functions. You will support the administrative aspect of the Technical Department taking responsibility for the day-to-day management and maintenance of some or all of the following: QMS, HACCP, Technical Reports, Non Conformance Logs, complaints, microbiological & nutritional surveillance; this work includes data entry, trending, information requests, co-ordination of actions, change management procedure and communicating to relevant parties. More ❯

of the Service Operating model, where more technical support is required Escalation of cases to level 3 where further support is required Investigation into quality complaints and escalation via QMS process to ensure resolution as per regulations Provide trouble shooting solutions to support customer queries and capture in local CRM to ensure trends can be monitored Support and training given More ❯