subsequent generation of a range of trials documentation/material. About You; You’ll have experience in firing trials and/or system integration & validation You’ll ideally have experience of external trials preparation and conduct You’ll be an excellent communicator possessing the ability to communicate with stakeholders at 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 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 more »
experience would be an advantage to this role: • At least 2 years’ experience in at least one of the following: Analytical method development and validation Risk assessment/Quality by Design. Vendor management of third party CMOs/CROs or experience working at a third party CMO or CRO. API more »
onto the QMS as necessary. Working alongside CMO’s and in-house specialists to support the production scaling activities. Create and implement QC and validation protocols, ensuring that regulatory processes are followed meticulously. Report any QC pass and fails, monitoring any non-conformance closely and taking corrective action. Strictly adhere 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 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 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 »
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 »
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 »
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 »
Help design and implement data governance processes and controls to ensure the quality, integrity, and security of master data. * Perform data profiling, cleansing, and validation activities to identify and resolve data quality issues and inconsistencies. * Action changes to master data in compliance with standards, validation rules, and governance processes. * Provide more »
facility. This opportunity offers a chance to expand your knowledge within manufacturing, aligning with our focus on future opportunities. Work packages such as Industrial Validation, manufacturing architecture, and principles of the factory of the future present challenging objectives for professional growth. What we're looking for: Completed a formal technical … will be identifying and resolving manufacturing problems across these projects. Provide support to existing manufacturing lines and facilitate new product introductions. Assist in industrial validation processes, employing tools such as FMEA's and process proving activities. Manage configuration control by incorporating design modifications into manufacturing documentation and industrial validation. Support more »
LEX is currently seeking a Verification and Validation Engineer who will actively engage in hands-on testing of the LEX diagnostic system. You will be working closely with the head of Quality and Engineering team and will be responsible for defining, designing, and executing verification and validation activities for the … read more about LEX here. You’ll develop testing strategies and methodologies with the wider LEX team to complete testing and draft verification and validation protocols. Your contributions will be crucial in ensuring the successful execution of validation and verification activities required ahead of regulatory approval and product launch. Responsibilities … include: Supporting with verification & validation to prepare the LEX System for 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 more »
from engine installation into test cells, along with fitting work and component changes, to running test programmes to engineering requirements in certification, performance and validation areas Duties and Responsibilities include, but may not be limited to: Fitting/Assemble of parts and components Using various hand, power tools and lifting … machines. Work on breakdowns and getting test cell to run again. Diagnose and fix a range of faults Run tests via software packages/Validation testing Work from engineering drawings (electrical, mechanical and hydraulic) Keep the work area clean, tidy and safe in line with 5S and total preventative maintenance 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 … the System/Business Owner and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a 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 … the System/Business Owner and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a more »
on validating the onboarding of new computerised systems to meet the needs of a rapidly growing customer base, as well as supporting the ongoing validation of expanding software systems. The position involves close collaboration with IT to establish data integrity requirements and evaluate the effectiveness of implemented solutions. Responsibilities: Support … the implementation of a risk-based approach to the validation of computerised systems to ensure compliance with Annex 11, 15 and GAMP 5. Preparing and execution of protocols for configuration, functional, end-to-end and user acceptance testing. Preparing and maintaining validation plans, assisting system owners with impact assessments, risk … assessments and identifying validation requirements for computerised systems projects. Assist in the authoring of User Requirement Specifications. Experience: Sufficient prior experience of validating computer systems in a Biopharmaceutical setting. A Degree (or equivalent experience) in a Science or related discipline . Experience in the validation of GxP software and Laboratory more »
As the selected Principal Hardware Engineer , you’ll join a small, but expert team where you’ll work on the design, development and validation of future communication products. Responsibilities for the role of Principal Hardware Engineer will include: Requirement specification and liaison with key stake holders throughout projects Design, development … of validation of high-speed application processors and supporting multiple high-speed interfaces Full lifecycle support of the current and future product lines Product compliance testing and product support As the selected Principal Hardware Engineer, your skills and experience should include: Experience designing boards to support high-speed processors Knowledge more »
My client is a deep-tech electronics company that produces advanced solutions combining mechanical, optical and software. Their products have already been used worldwide and are looking to expand further. They've grown by more than 11% in the last more »
Harlow, London, United Kingdom Hybrid / WFH Options
LinkPoint Resources Limited
and best practices Identify potential automation of existing processes within the ERP system Suggest solutions for operations and productivity enhancements Audit data and perform validation checks within the ERP system Report on KPIs and trends to support decision making Collaborate with internal and external teams and stakeholders Application Support Specialist more »
CM17, Old Harlow, Essex, United Kingdom Hybrid / WFH Options
LinkPoint Resources Limited
and best practices Identify potential automation of existing processes within the ERP system Suggest solutions for operations and productivity enhancements Audit data and perform validation checks within the ERP system Report on KPIs and trends to support decision making Collaborate with internal and external teams and stakeholders Application Support Specialist more »
a capability supporting developments across the full product life cycle. The team integrate real products, models and synthetic environments to provide visualisations, demonstrations, verification & validation as well as training capability and support. Responsibilities: • The role support the development of the worlds most advanced defence systems from the initial concept all more »
reporting and data sets which are interactive and user-friendly via PowerBI Identifying and integrating external data into the business data model Implementing data validation and cleansing procedures will ensure the quality, integrity, and dependability of the data. Improve the scalability, efficiency, and cost-effectiveness of data pipelines. Monitoring and more »
