1 to 25 of 36 Permanent QMS Jobs in the East of England

company procedures and policies to ensure smooth delivery of our service. Producing reporting on time and to agreed standards. Adhering to the companys quality management system and recycle correctly and responsibly. Required Skills: Experience in the installation, configuration and maintenance of access control and door entry systems. Basic IT Skills more »

IT systems at an advanced level, e.g. MS Office and Project, Atlassian JIRA and Confluence, etc. Experience of working within an ISO 9001 Quality Management System, or similar, is desirable. The above list outlines our ideal candidate, but we know some of you may not apply unless you qualify for more »

confidential use of patient information Desirable Use of Word and PC systems including operation of Windows-based software, and keyboard skills Use of quality management system Personal qualities Essential Ability to work to high standards under pressure. Flexible approach to working hours/duties Ability to work to strict standards more »

machines to manufacture precision components. Technical Adhere to Health and Safety regulations and law. Have knowledge of ISO9001, ISO14001 and Q1. Understand the Quality Management System Quality Brief. Responsible for the production of Company products. Achieve production targets and deadlines. Work from engineering drawings. Check materials for type and quantity. 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 »

a high profile Wind Farm project. You will be accountable for all Quality activities within assigned work packages, ensuring compliance with contractual requirements, project QMS, regulatory and legal requirements. The Quality advisor promotes and provides professional expert knowledge and guidance to managers, supervisors, and employees on quality practices, safety standards … in place to reduce the cost of poor quality and non-conformances within the project Duties Maintain quality expert knowledge on best practice and QMS requirements Supports the development and implementation of project quality assurance, management and control strategy Provides Quality support and direction to the Project team for assigned more »

all quality data is accurate and up to date. Implement quality control and assurance procedures to ensure that QA processes meet the companies established QMS and certification requirements. Assist senior management in preparing for and participate in external audits and regulatory inspections related to quality. As a successful candidate you more »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

quality reports on TrackWise Investigate OOS records in coordination with SMEs, and ensure the timely progression of reports. Participate in internal and external audits. QMS administration activities. What you'll need to succeed Our client is … looking for an individual with strong experience as a Quality Assurance Officer within a GMP Pharmaceutical/Cleanroom environment. Other key desirables include: Quality Management System activities and maintenance. Experience in participating in internal/external audits. Be able to work independently as well as within a cross-functional environment. more »

JIRA and Confluence, ERPs, etc. Desirable • Knowledge of using Agile/Scrum for delivering work packages • Experience of working within an ISO 9001 Quality Management System • A formal Project Management qualification (e.g. PRINCE2, MSP, PMQ, etc more »

the development and validation of biomarker assays and Precision Medicine Solutions. Facilitate/participate in projects to deliver improvements to the clinical laboratory Quality Management System through collaboration with R&D Understand the business needs of PM departments, with respect to technology infrastructure, third party work and human biological sample more »

the site Ensure that the HACCP (HACCP/TACCP VACCP) program is maintained and aligned with best practice at all times Ensure that the QMS is effectively implemented and amended to ensure product standards are maintained Ensure the QA and Hygiene teams are run effectively and adequate technical resources are more »

lab analysis Working closely with other sites for product specifications and documentation. Dealing with external stakeholders for food safety, quality and importing Maintenance of QMS Experience & Skills Required: The business is looking for an individual who has experience within the food industry. You must be able to lead, motivate and more »

will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in more »

leading pipeline. • Serve as the development and technical contact for customer teams, leading product issue and crisis management efforts to minimise business impact. • Utilise QMS data to monitor and review performance, taking appropriate action for improvement. • Stay ahead of technological developments, optimising systems and processes for a more cost-effective more »

United Living Group is a collection of four businesses dedicated to creating a connected, sustainable future: United Living Property Services: Revitalizing homes and communities through the regeneration of living spaces. United Living Infrastructure Services: Delivering resilient infrastructure for a stable more »

to expand and strengthen their skills, learning from expert colleagues from a variety of technical backgrounds. An excellent salary is on offer. Keywords: Quality, QMS, ISO, ISO:9001, 8D, PDCA, Continuous Improvement, Lead Auditor Another top job from ECM, the high-tech recruitment experts. Even if this job's not more »

clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and Biology teams working more »

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+ years of experience more »

ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators … Experience Degree in a relevant area of studies. 2 - 3 years’ experience in the role out of Quality policies. Knowledge of Quality Management Systems (QMS). Proven Auditing Skills. Continuous Improvement Mindset. Excellent interpersonal, verbal, and written communication skills. Experience of working at the headquarters of an international company. Fluent more »

Job summary An exciting opportunity has arisen to join a dynamic Blood Sciences Department as a Deputy Manager responsible for Haematology. You will play an important role in the operations teams working alongside managers responsible Biochemistry, Specimen Reception, Training and more »

trace testing Strong Excel knowledge and skills Attention to detail - quality controlling Experience within BRC - Supply chain assurance Must have experience in running a QMS Working Hours: Monday Friday 8am 4pm or 9am 5pm Role Overview: Be the technical and compliance contact for their customers, service providers and their growing … non- conforming products, product testing, finished product release, product recall, document control and customer complaints). Full authority on all aspects of the Quality Management System Salary Competitive salary offered, dependent on experience and skills 35 45k more »

strong focus on quality, you will guide and manage your team to enhance quality performance. Your main objective will be to strengthen the existing QMS and food safety systems, ensuring compliance with customer and business requirements and legislation. Working cross functionally, you will foster a shared commitment to upholding the more »

testing Strong Excel knowledge and skills Excellent attention to detail - quality controlling Experience within BRC - Supply chain assurance Must have experience in running a QMS 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 … Maintain processes, including GMP document control and training, needed for successful site compliance to the QMS. Participate in the review the performance of the QMS at planned intervals and provide regular reporting to ensure its continuing suitability, adequacy and effectiveness and propose improvements. Participate in the execution of a GMP … actions and a process to track their completion. Experience: Demonstrable experience in an Operational Quality Assurance role providing product impact assessments as part of QMS processes. Demonstrable experience in sterile manufacturing processes, ideally ATMP’s or biologics (Desirable). Previous exposure to R&D interfacing environment (Desirable). Demonstrable experience more »