1 to 10 of 10 Permanent QMS Jobs in Hampshire

range of responsibilities and duties with this role, as the Quality Assurance Engineer will be responsible for managing the EN9100 internal audits, maintaining the QMS, supporting continuous improvement and evaluating risk. The Quality Assurance Engineer will also be responsible for completing CAPAs with the audit team and participants. They will more »

across internal departments to provide Quality Assurance support. • Participation in external Quality audit activities. • Representing QA for various projects across the Basingstoke sites. • Key QMS processes – CAPA, Complaints, R&D QA, internal audits • Developing processes and providing training to R&D teams. What can we offer you? As Quality Assurance more »

from personal or Sonardyne work activities. To ensure awareness, understanding and adherence to all Sonardyne Policies and Procedures including Health & Safety, Anti Bribery, ISO9001-QMS and Operational requirements at all times. To take an active part in the Sonardyne Continuous Improvement Process, through providing suggestions for corrective actions, suggestions, initiatives more »

to management meetings. Committed team player. Able to work in a flexible, and occasionally highly demanding work environment. Awareness of a Quality Management System (QMS) Previous Military experience of benefit. Equal Opportunity Statement Lockheed Martin is proud to be an equal opportunity employer and is committed to maintaining a diverse more »

professional. The ideal candidate will have a strong background in Electronics manufacturing, RCA and Lean manufacturing Accountabilities Site Quality Control plan & Quality Management System (QMS). Site Calibration System. RMA Process (Problem solving, root cause analysis, trouble shooting, 8D). ISO 9001:2015 Accreditation. Customer Quality Supplier quality management. Responsibilities … company internal Quality Control Plan, driving improvement activities and carrying out quality risk assessments to continuously improve customer quality. Manage and maintain the company QMS ensuring ISO9001:2015 accreditation. Assist with internal Quality audits. Technical support for operators to be able to achieve daily production demand and Quality targets. Establishing more »

the internal calibration schedule and implementation of best practice into the business. Involvement with Design and Process FMEAs for new products and processes. Internal QMS Audits to support the internal audit team/programme. Post audit review meetings with Process Owners and follow-up review meetings. Assisting the Quality Team … with internal and External investigations and analysis, where required. Updating QMS procedures and their controlled release into the business. Data collection and analysis to support the business on-going Continuous Improvement Activities. Assisting with the weekly reporting and analysis of production scrap with a cross functional teams. Provide coaching and more »

driven to uphold standards, looking to hit the ground running and thrive in a collaborative environment, we want to speak with you! Responsibilities: Maintain QMS and ISO accreditation. Conduct internal audits. Support project teams in quality controls. Manage stakeholder communication and project monitoring. Ensure timely, cost-effective, and high-quality … project delivery. Foster positive relationships with stakeholders. Requirements: 3+ years' project support experience. Degree with relevant professional qualification. Demonstrated QMS maintenance and audit experience. Proven success in project support. Strong communication and stakeholder management skills. Adaptability and ability to manage multiple projects. Willingness to travel. Desirable: Membership in relevant professional more »

role include, but are not limited to: Ensure that the company complies with all relevant pharmaceutical regulations and guidelines. This includes maintaining the quality management system, conducting internal audits, and ensuring that products meet the necessary standards before release. Carry out the responsibilities of a UK Responsible Person as defined … senior management via the Quality Management Review. The correct candidate for this opportunity will have extensive GDP knowledge including working closely with a quality management system within the pharmaceutical distribution setting. The correct candidate will also be eligible act as a RP/RPi. If you are interested in this more »

Cure Talent is thrilled to partner with an innovative MedTech startup at the forefront of wearable medical device development and innovation. Due to continued growth, we have an exciting, newly created hybrid role for an NPI Engineer to join the more »

Cure Talent is thrilled to partner with an innovative MedTech start-up at the forefront of wearable medical device development and innovation. Due to continued growth, we have an exciting, newly created hybrid role for an NPI Engineer to join more »