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Lead Validation Engineer
Интересная позиция в крупной международной компании с сильной миссией. Удаленный формат работы в Великобритании и работа с передовыми научными технологиями делают вакансию очень привлекательной для экспертов в CSV.
Сложность вакансии
Роль требует глубоких экспертных знаний в узкоспециализированных стандартах (GAMP 5, 21 CFR Part 11) и опыта работы в регулируемых отраслях (Life Sciences). Высокая ответственность за аудит-готовность и необходимость совмещать классическую валидацию с современными инструментами автоматизации (Cypress).
Анализ зарплаты
Предлагаемая роль Lead уровня в сфере Life Sciences Software в Великобритании обычно оплачивается выше среднего по рынку QA из-за строгих регуляторных требований. Ожидаемый диапазон составляет £65,000 - £85,000 в год.
Сопроводительное письмо
I am writing to express my strong interest in the Lead Validation Engineer position at Dotmatics. With extensive experience in Computer System Validation (CSV) and a deep understanding of GAMP 5 and 21 CFR Part 11, I am eager to contribute to the validation of the Luma platform. My background in authoring IQ/OQ/PQ protocols and my familiarity with automated testing tools like Cypress align perfectly with your requirements for driving validation best practices in an Agile environment.
Throughout my career in the life sciences sector, I have successfully led validation activities for complex SaaS applications, ensuring full compliance with EU Annex 11 and ISO 9001 standards. I am particularly drawn to Dotmatics' mission of accelerating scientific innovation and would welcome the opportunity to mentor your validation team while maintaining audit-ready documentation. I am confident that my technical expertise and leadership skills will help Dotmatics continue to pioneer the future of digital science platforms.
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Описание вакансии
Our Why At Dotmatics
At Dotmatics, we believe science, data, and decision-making must be deeply intertwined for innovation to thrive.
Our Portfolio includes Luma, LumaLab Connect, ELN Platform, Graphpad Prism, Geneious, SnapGene, Protein Metrics, OMIQ, FCS Express, LabArchives, NQuery, EasyPanel, MStar, SoftGenetics and Virscidian.
We have a vision for a new Lab of the Future that will change the future of scientific research.
We have created the world’s most comprehensive digital science platform – best-of-breed software applications already used by more than 2 million scientists, together in a single ecosystem united by a powerful, flexible enterprise data platform. This is not flat data buried away in digital graveyards. This is dynamic, multi-dimensional decision-making.
Scientific enterprises need a new level of effectiveness to achieve tomorrow’s breakthroughs. Illness will not wait. The biosphere will not wait. We are tireless in our vision, because the time for innovation is now.
Shaping the Future of Science At Dotmatics
Our global team of more than 800 colleagues are dedicated to supporting our customers in over 180 countries. Together, with our scientific community of users, we accelerate scientific innovation in order to make the world a healthier, cleaner, and safer place to live.
You’ll join a collaborative, global team pushing the boundaries of scientific innovation. Your ideas and efforts will have a tangible impact, accelerating scientific progress and discovery. We offer a dynamic, remote-friendly environment that fosters high integrity and collaboration, empowering you to excel. Dotmatics is a company built by scientists, for scientists. Combined, we are now the world’s largest cloud-based scientific research R&D platform. We need your help to keep growing and pioneering the future.
We are Science Driven. We are Customer Centric. We are Better Together.
What do we need
As a Validation Lead, you will be responsible for leading validation activities for the Dotmatics Luma platform and its internal systems operating under GxP requirements. Serving as the subject matter expert for computer system validation (CSV) and ensures that software development, testing, and release activities comply with applicable regulations and standards including 21 CFR Part 11, EU Annex 11, GAMP 5, ICH Q10, and ISO 9001 as applicable.
The Validation Lead partners closely with Product, Engineering, and Quality Management teams to drive validation best practices throughout the software development lifecycle (SDLC), ensuring traceable, audit ready deliverables that meet customer and regulatory expectations.
In this role you will get to:
- Author, review, and approve validation lifecycle documentation including Validation Master Plans, URS, FRS, Traceability Matrix, Risk Assessments, IQ, OQ, PQ protocols and reports following GAMP 5 principles, including risk-based approaches to validation activities
- Working with the software quality team and devops to leverage automated tools such as Cypress to develop, review and run IQ, OQ, and PQ protocols.
- Apply GAMP 5 framework to determine appropriate validation strategies and documentation requirements.
- Mentor/lead junior validation team members and QA staff on validation methodologies and documentation best practices.
- Coordinate and execute validation testing activities, manage defect identification, impact assessment, and resolution.
- Serve as Luma subject matter expert for GAMP5, 21 CFR Part, EU Annex 11, and applicable ISO standards.
- Provide validation guidance and training to engineers, QA analysts, and project managers on CSV principles, IQ/OQ/PQ expectations, and 21 CFR Part 11 controls.
We are looking for people who can support customer-facing validation activities, assist with CAPA investigations and audit responses, and collaborate with the Quality Management team to maintain document control, periodic reviews, and overall audit readiness for validation artefacts.
The key skills we are looking for:
- Deep working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and GxP requirements as they apply to software systems
- Familiarity with ISO 9001quality management system principles
- Demonstrated experience authoring and executing IQ/OQ/PQ protocols, traceability matrices, and validation summary reports, including use of automated testing tools (e.g., Cypress, Playwright) to generate and capture test evidence
- Understanding of software development lifecycle (SDLC) and Agile methodologies.
- Experience with validation of cloud-based systems, SaaS applications, or commercial off-the-shelf (COTS) software
You may also have:
- Bachelor’s degree in Computer Science, Biology, Chemistry, Engineering, or a related field (preferred but not required).
- Background in regulated life sciences environments, such as pharmaceutical, biotech, or medical device industries.
Research shows us theconfidence gap and imposter syndrome can get in the way of meeting outstanding candidates, so please don’t hesitate to apply — we’d love to hear from you.
By submitting your application, you agree that Dotmatics may collect your personal data for recruiting, global organization planning, and related purposes. Dotmatics Privacy Notice explains what personal information we may process, where we may process your personal information, our purposes for processing your personal information, and the rights you can exercise over Dotmatics use of your personal information.
Dotmatics is an equal opportunity employer. We are a welcoming place for everyone, and we do our best to make sure all people feel supported and connected at work.
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Навыки
- Computer System Validation
- GAMP 5
- 21 CFR Part 11
- EU Annex 11
- GxP
- ISO 9001
- Cypress
- Playwright
- SDLC
- Agile
- SaaS
- Quality Management
Возможные вопросы на собеседовании
Проверка фундаментальных знаний стандартов, критически важных для данной роли.
Как вы применяете риск-ориентированный подход GAMP 5 при планировании валидации новой облачной платформы?
Оценка опыта работы с современными инструментами в контексте GxP.
Каким образом вы интегрируете результаты автоматизированных тестов (например, из Cypress) в валидационную документацию для обеспечения прослеживаемости?
Важно понять, как кандидат справляется с несоответствиями в регулируемой среде.
Опишите ваш опыт управления дефектами, обнаруженными во время выполнения протоколов OQ/PQ. Как вы оцениваете их влияние на статус валидации?
Роль подразумевает лидерство и обучение других сотрудников.
Как вы подходите к обучению инженеров и QA-специалистов принципам CSV, если они ранее работали только в нерегулируемых средах?
Проверка готовности к внешним проверкам.
Расскажите о вашем опыте участия в регуляторных аудитах. Какие аспекты валидационной мастер-плана (VMP) обычно вызывают больше всего вопросов у аудиторов?
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