1 to 25 of 43 QA Jobs in Hertfordshire

the ongoing growth of the business Developing clean code which adheres to SOLID principles and following the solution architecture Ensuring that the application lifecycle, quality assurance, database engineering and build and deployment tasks are in place and understood by the team Ensuring that the business has systems that are performant more »

input, product strategy and internal operational requirements. Garner estimates all assigned work for client approval Outline high-level solution design to lead developers and QA analysts Build and accurately document requirements for new developments and versions for software delivery, and functional requirements for agile and/or waterfall software development. more »

and feedback to the wider business on customer experience. Contribute to deliver Thrives customer ambition. Requirements: Technical expertise in complaint management, customer service, and quality assurance is essential. Ability to role model our core behaviours, with a focus on trust and respect for everyone. Excellent communication and interpersonal skills. Strong more »

the General Contractors Services lead on site. The Technical Manager will cover the prescribed region and support creation of standardised systems controls requirements, schedules, QA/QC and reporting standards. This role can be based in either the UK, Germany or Netherlands with 35 % travel required. Your responsibilities Collaborate with more »

responsive design, mobile web development, performance optimisation, accessibility and sustainability. Experience working with a wider technical team such as Experience Design, Business Analysts and Quality Assurance providing support and direction alongside the Lead UI Developer. Experience of digital products using Digital Experience Platforms (such as Optimizely, Adobe, Sitecore, Acquia or more »

with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all more »

with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all more »

and schedules, ensuring projects remain on track and within budget. Team Leadership: Lead and motivate project teams, fostering a collaborative and productive work environment. Quality Assurance: Ensure that all project deliverables meet the required quality standards. Reporting: Prepare and present regular project status reports to senior management and other stakeholders. more »

and schedules, ensuring projects remain on track and within budget. Team Leadership: Lead and motivate project teams, fostering a collaborative and productive work environment. Quality Assurance: Ensure that all project deliverables meet the required quality standards. Reporting: Prepare and present regular project status reports to senior management and other stakeholders. more »

won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from more »

won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from more »

won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from more »

Borehamwood, Office based | Wholesale The successful candidate will be responsible for ensuring all processes under Good Manufacturing and Good Distribution Practices are maintained and supporting and deputising in the absence of the Responsible Person for import (RPi)To support the more »

UK Power Networks & SSEN Contracts in Stevenage . As a Project Manager youll be responsible for coordinating and managing people, plant, materials, budget, programme, quality assurance, contract requirements, and health & Safety of employees and general public. MES is proud to be a key partner on the UKPN ED1SON Alliance & SSEN more »

ourUK Power Networks & SSEN Contracts in Stevenage. As a Project Manager you’ll be responsible for coordinating and managing people, plant, materials, budget, programme, quality assurance, contract requirements, and health & Safety of employees and general public. MES is proud to be a key partner on the UKPN ED1SON Alliance & SSEN more »

ongoing projects and cover contracts with UK Power Networks and SSE. Responsibilities of the Project Manager: Coordinating and managing people, plant, materials, budget, programme, quality assurance, contract requirements, and health & Safety of employees and general public Delivering substation build and refurbishment works across the East of England including design, project more »

and devices to communicate effectively with the control panels. and resolve any communication or integration issues between control panels and the BMS. Testing and Quality Assurance: thorough testing of control panels to ensure functionality and adherence to specifications. quality checks on completed panels to verify compliance with industry standards and more »

with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all more »

the technical content of work packages associated with allocated projects, in liaison with supply chain contacts in CSC (Clinical Interface), R&D Procurement, External Quality Assurance (EQA) and external TPC contacts. Input technical expertise and TPC oversight at all stages of the work packages. Work package scope: primary and secondary more »

with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all more »

correlating with equipment models. Conduct data mining activities and generate insightful reports. Provide occasional on-site assistance for biomedical equipment repairs. Ensure compliance with quality assurance and safety policies. Undertake additional tasks assigned by the Technical Support Manager. Travel across the UK for operational duties and training sessions as required. more »

development and implementation for AV and Digital Media systems and services across the organisation. (This work includes planning and scheduling, documentation, source code control, quality assurance, maintenance, error tracking and reporting, standards and guidelines, release, technical user support and new product research and development). To provide the technical advice more »

development and implementation for AV and Digital Media systems and services across the organisation. (This work includes planning and scheduling, documentation, source code control, quality assurance, maintenance, error tracking and reporting, standards and guidelines, release, technical user support and new product research and development). • To provide the technical advice more »

Copello has partnered with a leading defence company who specialise in the design and manufacture of advance systems for air, land and sea applications. The company are currently looking to hire a Product Assurance Engineer to join the quality supply more »

Quality Co-Ordinator to work across a number of our key framework clients. As the Quality Co-Ordinator, you will be part of our Quality Assurance team who are responsible in ensuring its construction outputs meet the quality standards set. As the Quality Co-Ordinator your responsibilities will include: Ensuring more »