76 to 100 of 128 Permanent Validation Jobs in the East of England

and partition in-house designs and IP from third parties and wrap with modelling logic to represent mixed signal design element. Asist with the validation of new silicon chips with a mix between CI/CD automation and manual tests through electrical test equipment. Qualifications and Experience: Strong experience in more »

in maintaining due diligence in the technical function. Updating QMS, accurate and up to date and accurate specifications. Supplier due diligence (supplier audits) HACCP validation which includes checking, providing, and validating legal info on the printed packaging.Role Responsibilities: Quality management systems: HACCP team works with technical manager. Updating of QMS more »

PM Group is seeking a Validation Engineer to join an API Manufacturing facility in Suffolk for 3-4 months. Responsibilities: Work closing with Capital Project, Production, QA, and R&D departments to get the validation scopes and agreements to release the desired production status in the agreed timelines. Weekly update … to report the progress status of the validation works. Update and draft the required validation documentation, including but not limited to CSV/CQV validation protocols, VP, C&QP, SIA, URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR. Execution and approval of the corresponding protocols to release … the required equipment for GMP production Weekly Validation Report Draft, execution, and approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects in the pharmaceutical and/or biopharmaceutical sectors. Working with other departments and key stakeholders Good communication skills and be more »

YYYY First name (Required) Surname (Required) Email (Required) Phone (Required) Message Attach CV (Required) Max. file size: 1 MB. Email This field is for validation purposes and should be left unchanged. 6 Months initially with a view to extend Seen a job for someone you know? Refer a friend today more »

be responsible for: the data management of clinical trials developing and maintaining a clinical database (experience with OpenClinica is a plus!) the design and validation of CRF specifications the data strategy through risk assessments related to data management This role is for you if you possess: data management experience within more »

the on-going success of this ever growing business. DUTIES & RESPONSIBILITIES: Oversee the commissioning process for new repeat-build machines. Supervise the installation and validation of upgrades on machines. Document Overall Equipment Effectiveness. Develop and update related documentation. Manage and revise logs of machine settings and modifications. Analyze machine performance more »

to join our highly skilled and dynamic Test Equipment Design Team. In this stimulating and rewarding role, you will support the design, integration, and validation of test system hardware solutions while advancing your career along an exciting path. As a Principal Hardware Design Engineer, your responsibilities will include defining and more »

out design activities related to innovative technologies, cost optimisation and break through ideas related to BEV vehicles. Studying technical, build business case and lead validation and adoption of the new design. Leading/supporting communication and negotiation with internal and external stakeholders. Skills and experience required for the Body Engineer more »

out design activities related to innovative technologies, cost optimisation and break through ideas related to BEV vehicles. Studying technical, build business case and lead validation and adoption of the new design. Leading/supporting communication and negotiation with internal and external stakeholders. Skills and experience required for the Body Engineer more »

and partition in-house designs and IP from third parties and wrap with modelling logic to represent mixed signal design element. Asist with the validation of new silicon chips with a mix between CI/CD automation and manual tests through electrical test equipment. Qualifications and Experience: Strong experience in more »

sensor loop Signal conditioning for sensors and initiating elements Failure modes and actuation methods for solenoid valves and final elements Proof testing and maintenance Validation of C&E Management of Fire and Gas Systems identify the procedures and standards involved in managing Fire and Gas systems both offshore and onshore. more »

Trust. To support further implementation and ongoing management of an Electronic Prescribing and Administration system (EPMA) at the Trust To collaborate with the configuration, validation, testing and rollout of digital systems from a pharmacy perspective To assist with the formulary build and continued maintenance and development of the EPMA system more »

CK Group are recruiting for a Validation Manager on behalf of a growing Cell Therapy CDMO to be based at their site in Cambridge on a permanent basis. The Role: Reporting to the Head of Quality, you will be responsible for leading the Validation function by building the team and … with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements Responsibilities : Manage a team and ensure validation master plans (VMPs), protocols and procedures are established To prepare and maintain validation plans (VPs) and identifying validation requirements. Assist in the authoring of User … Requirement Specifications, DQ/IQ/OQ/PQ protocols, and reports for validation purposes. Working with external companies and project teams to ensure activities that require specialist knowledge are completed Executing validation protocols for equipment, facilities and utilities Your Background: Degree (or equivalent) in a Science or related discipline more »

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 stages of … a stimulating environment, with a lot of opportunities for your professional and personal development. Job Summary We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified … and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with cross-functional teams to ensure the successful implementation of CQV more »

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 stages of … a stimulating environment, with a lot of opportunities for your professional and personal development. Job Summary We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified … and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with cross-functional teams to ensure the successful implementation of CQV more »

projects in the most innovative companies. Join us and start building tomorrow’s world today! Job Description We are seeking a highly skilled Software Validation And Verification Engineer to join our Basildon team in the defence sector. The role is hybrid and due to the nature of the defence industry … successful applicant to be a sole British citizen eligible for security clearance Key roles and responsibilities: HSI and Rig Testing: Conduct thorough testing and validation activities related to Human-System Interface and rig testing for missile system software. Automated Testing: Implement and execute automated testing methodologies to ensure the reliability … defect tracking and resolution. Collaborative Tools: Utilise collaborative tools such as Jira and Confluence for effective project management and communication. Qualifications Experience in software validation and verification, particularly in the defence industry. Proficiency in HSI and rig testing methodologies. Strong understanding of automated testing techniques and methodologies. Familiarity with DO178 more »

Great opportunity for a Validation Engineer to join a leading UK technology manufacturing company that offers excellent training, support, and career development. This new role will suit a ‘hands-on’ Validation Engineer who will enjoy a broad role in a small specialist team working on complex printing equipment (electrical elements … . The role will involve setting up, running, fault finding/problem solving and interpreting the results of a broad variety of hardware product validation projects. The Opportunity Linx Printing Technologies designs and manufactures innovative industrial printing and laser coding equipment used to mark batch info and consumption dates on … packaging within food & beverage, pharmaceutical and related sectors. Based 3-4 days a week at the Linx HQ in PE27 5JL, the Validation Engineer will be part of a small, newly created ‘Value Analysis & Value Engineering’ team looking to drive product cost reduction without sacrificing performance and quality. The specialist more »

Join an innovative and well-funded company as Verification and Validation Engineer, contributing to the development and refinement of cutting-edge diagnostic systems. Your role will be pivotal in perfecting the electronics design of the product as they move towards launch. You'll work closely with the team and collaborate … with an external electronics team to ensure smooth knowledge transfer, design integrity, and technical evaluations. Position Overview They are looking for a Verification and Validation Engineer to join the team. You will be responsible for defining, designing, and executing verification and validation activities, ensuring our diagnostic systems meet regulatory requirements … and are ready for product launch. Key Responsibilities Support verification and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering more »

A wireless communications company based in Chelmsford is seeking a Validation Engineer to join their team. As a Validation Engineer you will have a number of responsibilities that include; RF and electronics testing Automated test development Analysing test performance PCB debug+development Develop test solutions for ICs and PCBs To be … considered for the Validation Engineer vacancy you must have: 2-4 years of experience in a relevant role Experience with Python Experience with RF/electronics test and measurement equipment PCB debugging and test experience Good digital electronics knowledge Experience with Altium for PCB design/development A passion for … valid driving license to apply for this position. The office is not accessible by public transport. If you have interest in applying to the Validation Engineer vacancy or would like further information, please contact Roberta Wright. more »

A leading manufacturer of industrial off-highway diesel engines is currently looking for a Validation Engineer to join the team at their site based in Peterborough. The position is paying up to £30.62 per hour based on a 37 hour week. As a Validation Engineer, you will report to the … Validation Engineering Manager. You will have responsibility for conducting testing on validation test beds to sign-o... more »

processes Lead all manufacturing requirements and processes required for AC/DC designs, including such processes as FMEA, DFM/DFA and Verification and Validation plans/reports Carrying out feasibility studies for new technical innovations. Supporting test engineers to carry out testing where required. Test, Develop and verify design … policies & process. Writing test plans to a high standard and in place before any testing conducted with reports completed aligned with the verification and validation process. Contributing to the ongoing improvement of the standard design process. Accountabilities Ensure company standards are met for hardware designs, both regulatory & practice, both in … a product development environment, familiar with New Product Introduction (NPI) Primary Design Review (PDR), Critical Design Review (CDR), First Article Inspection (FAI) Verification and Validation (V&V) In depth knowledge of both theoretical and practical aspects of electronic engineering Understanding of firmware design & control considerations needed when developing hardware which more »

of software operating/automation systems, including, but not limited to, utility, development, and diagnostic software. They perform technical planning, system integration, verification and validation, cost, risk, supportability and effectiveness analyses for total systems. The Embedded Software Engineer will report to the Electronic and Sensor Integration Manager, Energy and will … MV & HV applications. Responsibilities: All aspects of the software development life cycle: Requirements capture Feasibility study and architecture definition Software design & implementation Integration and validation test Firmware development Design and implement embedded software Implementing hardware drivers, interfaces, abstractions, state machines, advanced signal processing algorithms, application modules and unit tests What more »

the maintenance of the Pharmaceutical Quality Systems within the technical services department To ensure maintenance of the pharmacy manufacturing unit facilities (including monitoring, calibration, validation and general maintenance) is carried out About us There has never been a more exciting time to join West Hertfordshire Teaching Hospitals NHS Trust! Major … Essential Understanding of the principles of GMP and QA in Aseptics/Production manufacturing environment Understanding of Pharmaceutical Quality Systems Knowledge of Audit and validation Computer and IT competent COSHH Regulations and Health and Safety at Work Act Need for confidentiality Good Dispensing Practice Desirable Familiar with chemotherapy regimens EMIS more »

NPU System Performance Modelling Engineer in Cambridge, UK About Neubla As pioneers of innovative neural computing, Neubla is transforming the future of computing by bringing the enormous potential of neural computing to the highest performance in most data-intensive applications. more »

in developing and updating the database tool, collaborating with the development team, or providing direct support for Java-based solutions. Develop and formalize the validation plan for database tools and content. Perform validation of database tools. Provide database documentation for Project Reviews. if you are currently looking to take the more »