1 to 25 of 29 Permanent QMS Jobs in the East of England

systems and assurance, with relevant QHSSE experience in a manufacturing and/or project environment. Experience in the implementation and maintenance of a Quality Management System/ISO certification is essential. You are well organised, with good analytical and critical thinking skills, and excellent verbal and written communication skills. You more »

files and documentation for new products, working closely with Sales and Purchasing to resolve technical questions. Requirements: Experience in document control for ISO9001 Quality Management System and understanding of medical regulatory standards. Excellent computer literacy with proficiency in Microsoft Office products is essential (especially Word and Excel). NetSuite and 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 »

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 »

management of employee performance, absence management, and management of rostering Accountability for the clinical safety of the transfusion service, and operation of the quality management system, including compliance with the Blood Safety and Quality Regulations 2005 (as amended) and BS EN ISO 15189:2012 Liaison with the client, Mid and 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 »

FID experience (general - Gas Chromatography experience will be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT more »

opportunity with a clinical-stage biopharmaceutical company with multiple Phase 3 assets.Key Responsibilities:To play a key role in maintaining and monitoring the GxP QMS ensuring it meets all regulatory requirements and standards, with emphasis on GCP compliance.To provide support and advice to Clinical Development teams with regards to:Definition 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 »

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 »

and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development. Requirements: Bachelor's degree more »

procedures, and prepare comprehensive reports in accordance with design control standards.Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485)Knowledge in mechanical engineering with a focus on testing equipment and innovation in product development.Requirements:Bachelor's degree in more »

/FDA regulated environment. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Collaborate with the Engineering and quality departments to ensure test method, equipment and materials are available in line with company timelines. Analyse and 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 »

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 »

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 »

for a perm role on behalf of our client based in Stanford le Hope. Duties and Responsibilities: Maintain the company's Environmental and Quality Management System frame work and ensure ongoing compliance with accredited ISO90001, ISO14001 and any other ISO standards as applicable. Manage day to day operation of the more »

knowledge, a minimum of 3 GCSEs. Experience of working in a Biomedical laboratory. Knowledge of computer applications in use within Pathology, particularly LIMS, Quality Management System and Procurement system. High degree of dexterity required Working knowledge of the receipt and preparation of samples for biomedical testing. Desirable Science A Levels 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 »

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 »

Are you an experienced QMS Administrator looking for a part time role? If so, this interesting and flexible role could be just what you are looking for. The Client Established in the UK in 2000, but originally developed in California, USA, our client designs and manufactures a range of PH … renowned companies who are leaders in their specialised field. The Role They are now looking for an experienced QMS Administrator to ensure the Quality Management System processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys quality management system (QMS) to ensure compliance with ISO 9001 and more »

include developing and building quality frameworks for all stages of project development and manufacture through the management of a digital document quality management system (QMS). This will require good communication skills to get buy-in from all stakeholders. Requirements: Graduated with a bachelor's or master's in engineering 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 »

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 »

development. The post holder is expected to take a role in data analytics within the department and play a major role in the departments QMS system. They will also be expected to undertake method development, protocol development and clinical liaison including 'duty' biochemist roles for clinical advice for Trust Doctors … and to GPs as required on matters concerned with patient management. The post holder will assist in the delivery of the Quality Management System (QMS) for Chemical Pathology and ensure high quality service delivery. Person Specification Your application will be scored against the JD/Person Specification Essential 0 - does more »