specifications. Maintain cleanliness and organisation in the work environment. Report to Unit Manager promptly regarding any issues or delays. Adhere to company's qualitymanagementsystem and health & safety protocols. Skills & Attributes: Experience in engineering or related field preferred. Proficiency in using precision measuring equipment. Adaptability and quick learning abilities. more »
Employment Type: Permanent
Salary: From £13 to £16 per hour Negotiable dependant on experience
Northallerton, North Yorkshire, Yorkshire, United Kingdom
North Yorkshire Police
applications to the post of Digital Forensic Technician. In this role you will support the Technical Manager with the ongoing development of the QualityManagementSystem and technical functions within the Digital Forensics Unit (DFU). You will also assist in the development and maintenance of Technical Standard Operating Procedures more »
knowledge, a minimum of 3 GCSEs. Experience of working in a Biomedical laboratory. Knowledge of computer applications in use within Pathology, particularly LIMS, QualityManagementSystem 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 »
ADR Transport Regulations for example). Desirable Specialist Knowledge of MRI Specialist knowledge of UV Experience of teaching and training others Working knowledge of QMS Understanding of HR policies and procedures Skills/Attributes Essential Able to act as a Trust expert in areas of specialist expertise and communicate to more »
the team and with external partners. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and QualityManagementSystem, compliant with ISO standards PERSON SPECIFICATION Required Experience Good understanding of communications, wiring systems and schematics or equivalent Experience with inspection and testing– C more »
house and contract engineers in Mechanical Engineering Creation and management of product and production Technical Documentation Manage and maintain engineering data within ISO 13485 QMS Engineering management of operations – Design Change, Compliance, Validation etc. Take ownership of engineering drawings and technical documentation relating to technical files Skills, Experience and Education more »
business * Basic recognition of components is desirable, but not essential * Previous experience in an electromechanical production environment is desirable * Working experience of ISO 9001 QMS * A positive, can do attitude 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 »
Bedford, Bedfordshire, South East, United Kingdom Hybrid / WFH Options
Ten2Two Ltd
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 QualityManagementSystem processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys qualitymanagementsystem (QMS) to ensure compliance with ISO 9001 and more »
Senior Quality Engineer, Quality Manager The Role Reporting into the Quality Manager you will have the following duties: -Supporting the implementation of the qualitymanagementsystem throughout the site. -Maintaining the quality manuals and quality procedures. -Conduct qualitysystem audits and assist in training. -Support and lead process improvements. The more »
QP qualification essential Significant experience working as in a senior quality role within solid dose and none - sterile liquid pharmaceutical settings working and implementing QMS strategies. Significant experience working with cGxP regulations Previous management/supervisory experience in a quality setting Important Information: We endeavour to process your personal data more »
our cutting-edge Medical Imaging Devices. Your tasks will encompass overseeing change management, validation and verification, systems engineering guidance and adherence to our QualityManagementSystem standards. The ideal candidate would be an experienced systems engineer/manager who has experience working on hardware heavy devices. Any experience with optics more »
The role involves coordinating and managing all QA/QC activities to ensure compliance with quality standards and client specifications according to the Company QMS, with appropriate record-keeping. Quality control and assurance of purchased, fabricated, and completed products. Drive to continually improve the standard of quality compliance and awareness more »
division within the QA department. a small team of quality professionals, supporting with development and training. You will be responsible for: the businesses qualitymanagementsystem is maintained to a high standard and aligns with regulations. CQA oversight and support to Pre-Clinical and Clinical Operations. and host regulatory inspections more »
Cheltenham, Gloucestershire, South West, United Kingdom
Jefferson Wells
/Warehousing Team in daily Dock to Stock Processing. Receive, verify, process and receipt goods to the business system. Process through the Quality database (QMS) Record supplier C of C's/Pack slips Communicate queries through to appropriate person. Transact, verify and locate Inventory. Comply with Stores Procedures Physical more »
burr components. - Running and checking “1st” off and random batch inspection. - Observe machine operation to verify accuracy of machine settings. Technical Understand the QualityManagementSystemQuality Brief. Responsible for the production of Company products. Achieve production targets and deadlines. Work from engineering drawings. To clock in/out and more »
Hatfield, Hertfordshire, South East, United Kingdom
RGE Services Ltd
company procedures and policies to ensure smooth delivery of our service. Producing reporting on time and to agreed standards. Adhering to the companys qualitymanagementsystem 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 »
Manager with the development of safe systems of work Quality - To instill best working practices. Ensure that all Operational & Technical Procedures per the QualityManagementsystem are strictly adhered to, escalating any issues to the UK Facilities Manager. Requirements Essential Full, formal electrical apprenticeship Gold Card Good customer and leadership more »
PDA reports ensuring that it is correctly completed and procedures are followed within the required timescales - Work in line with the Company’s qualitymanagementsystem, industry standards and regulations and Health & Safety policy - Understand the importance of GDPR and the protection of sensitive customer information Professional Requirements: - Have a more »
was you? AWE is currently recruiting for a Commissioning Engineer to provide due governance and management to meet specifications and acceptance criteria, within the QMS and Project Delivery processes and procedures, whilst organising and managing commissioning activities. Location: Reading area Package: £33,850 - c£44,000 (depending on your suitability more »
being the first concern and focus. Ensure everyone works in the safest of environments and takes responsibility for their own and others safety. Use QMS documentation and tolls to control standards, proactively identify skills and knowledge gaps to ensure safety levels are maintained. Design and deliver multiple projects, commercially aware more »
for a Senior Clinical Quality Assurance Specialist to join a well established QA function. KEY RESPONSIBILITIES: Coordinating the implementation of the company's qualitymanagementsystem pertaining to Good Clinical Practice (GCP), including oversight of external vendors, training on quality procedures, and performance monitoring against established standards. Serving as the … and Clinical Plans. Writing and/or reviewing QualityManagementSystem (QMS) documents, including SOPs. Acting as the system administrator for the electronic QualityManagementSystem (eQMS) and managing documents within the system on a day-to-day basis. Generating and monitoring quality metrics, including those derived from the eQMS. … practices related to GCP and GCLP, with an understanding of considerations for Advanced Therapy Medicinal Products (ATMPs). Skilled in maintaining and monitoring a QMS, preferably in a small/start-up organization environment. Educational Requirements: Bachelor's Degree in Life Sciences, Pharmacy, or Regulatory. Understanding of immunology is desirable. more »
job description carefully before applying, thank you) Primary Objectives: The Quality Assurance Associate is responsible for helping to maintain and improve the DnaNudge QualityManagementSystem as part of the Quality team by identifying potential improvements and efficiencies and helping to develop, revise and implement Quality procedures and policies. The … compliance of all regulatory requirements. Participate in the execution and support of internal and external regulatory audits and inspections. Support the maintenance of DnaNudge QMS program ensuring all processes are compliant to the relevant standards. · Manage some DnaNudge documentation associated with the QMS where required · Perform initial quality reviews of … internal auditor · (Desirable) Has worked in a similar role within the Medical Device/Pharmaceutical industry · (Desirable) Working knowledge and experience with a QualityManagementSystem, such as deviations, investigations, CAPA, and customer complaints. · (Desirable) Experience of ISO certified QMS (ISO13485) Knowledge (Essential) In depth understanding of approaches to qualitymore »
Lead to join our Quality Team based in Coventry. Duties & Responsibilities As a Quality & Improvement Lead you will: Develop a project level QMS (QualityManagementSystem), in line with the business QMS, specific to customer needs and provide process owners with support to devise and establish sector quality procedures, standards more »
highly skilled team that will invest in your on going professional development. The Role: *Working as part of a team of 2, overseeing the QMS systems and advocating improvements and championing processes *Hands on Mechanical Inspections to ensure quality is achieved *Further technical training such as Internal Auditor training and more »