1 to 25 of 33 Permanent QMS Jobs in the East of England

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 »

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 »

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 »

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 »

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 »

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 »

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 »

implementing our Food Safety. Quality and Hygiene systems in line with business growth and development. The role will be responsible for ensuring the company QMS is maintained and up to date. Ensuring compliance with BRC and Customer technical standards/codes of practice. Key responsibilities : Goods in checks. Paperwork checking 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 »

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 »

ready to step up into a Principal role or an established PA looking for a change in their career. The Role: Adherence to the QMS including root cause analysis and communicating with clients on technical matters. Assistance in maintenance programs for the Departments specific analytical instrumentation and any other analytical 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 »

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 »

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 »

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 »

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 »

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 »

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 »

Q-Pulse system, in conjunction with the quality & training manager. The post holder will implement a high quality, efficient and effective Quality Management System [QMS], Training Programme, monitoring quality and training process using key performance indicators. They will be responsible for operational activities as outlined within the QMS. In conjunction … CLINICAL GOVERNANCE AND QUALITY To be responsible for the implementation of UKAS, MHRA, HTA and HSE standards for quality & training using the pathology Quality Management System as established, to fulfil the quality & training circles and audit inherent to the ISO 15189 standards of compliance. In conjunction with the quality & training 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 »