5 Quality Management Jobs in Stevenage

complex systems for use in the defence sector globally. This is a fantastic opportunity to join a company that pride themselves on delivering high quality superior products to their sector. Job Role – Principal Product Assurance Engineer (Supply Chain) The Principal Product Assurance Engineer shall join the Quality Supply … Chain team in support of non-conformance management and audit of the production supply chain. Duties – Principal Product Assurance Engineer (Supply Chain) • Handle major equipment supplier Product Non Conformance. • Facilitate implementation of the non-conformance defect investigation process with the supplier to ensure that adequate and appropriate corrective actions … are implemented. • Provide supplier Non-Conformance data analysis and summary reports. • Identification of improvements with respect to the supplier non-conformance management process and its implementation within SAP. • Conduct Quality audits/assessments. • Opportunity to identify process improvements to aid on time and on quality delivery of more »

The role of Associate Director, Precision Medicine Quality & Design, will be to support the development and validation of biomarker assays and Precision Medicine Solutions. In addition, they will be responsible for supporting the Head of Precision Medicine Quality & Design in the development of a systematic quality risk … management program for Precision Medicine (PM) across multiple areas, including “fit-for-purpose” assay validation, regulatory risk, human biological samples, data disclosure, anti-bribery and corruption, privacy and most importantly, GCP. The Associate Director PM Quality & Design will ensure Precision Medicine strategies on and operations within programs they … support are compliant with GSK policies and procedures and regulatory requirements. The role covers a wide scope of operational quality and compliance responsibilities, from Ph1 through to launch. As Associate Director, Precision Medicine Quality & Design, you will work effectively in a matrix across PM business functions to ensure more »

The Quality Assurance Specialist will be responsible for ensuring the standards of the Quality Management System (QMS) at CGT Catapult Stevenage are maintained in a fit for purpose state of control, and improved, for a multi-purpose, multi-client facility. This will involve maintenance and improvement of … associated procedures for controlling key quality and business processes in addition to helping develop the measures and governance structures to be employed to maintain visibility on the processes and interactions within and across them. The Quality Assurance Specialist will also be responsible for managing the Quality interactions … between CGT Catapult and our Collaborators and will be the primary Quality point of contact for a defined Collaborator. Reporting to and with the guidance of the Quality Assurance Lead, this role will ensure that CGT Catapult Stevenage, via proactive engagement, meets the standards and expectations of two more »

be responsible for collating and reporting activity completion and earned value data to support the commercial team, as well as key performance data for quality management purposes. As the Planner your responsibilities will include: Develop strong working relationships with clients, consultants, sub-contractors and external parties to ensure … at all relevant levels aware of programme risks, key issues and solutions in a proactive manner Provision of reports and progress information to senior management and clients in line with MES and client requirements Skills & Knowledge Requirements Demonstrable systems/tools experience - Primavera P6 and Microsoft Office suite Experience … of planning on a variety of engineering projects Previous experience of electrical transmission projects Previous relevant project management and costing experience within the HV electrical sector Good working knowledge of NEC3 contracts or similar Able to facilitate and lead on the development of schedules with stakeholders at all levels more »

Work with the existing software development team. Follow all relevant medical device directives and EU GMP Annex 11 with regards to software. Keep relevant Quality Management System documentation up to date. Qualifications & Experience: 2+ years of experience creating software for a regulated field such as medical devices. 2+ more »