technology transferroot cause analysisprocess validationcgmpmultivariate data analysischemometricsprocess analytical technologynir spectroscopy
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Роль чётко описана и включает практическую работу с PAT, валидацией и улучшением производства в международной медицинской компании; при оценке важно учитывать работу на площадке и требование гибкости.
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Понятные задачи
Международная команда
Фармацевтика и здоровье
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
PAT Specialist (Pharmaceutical Manufacturing): Supporting process analytical technology for inline production, drug substance and drug product manufacturing, and real-time release with an accent on NIR spectroscopy, process data, control strategies, and PAT measurement models. Focus on implementing PAT projects, investigating process issues through root-cause and multivariate analysis, and facilitating technology transfer, validation, and equipment qualification.
Location: Cramlington, Northumberland, United Kingdom; onsite at a pharmaceutical manufacturing site
Company
hirify.global is a global healthcare company focused on women’s health, biosimilars, and other health solutions.
What you will do
Provide Process Analytical Technology (PAT) support for inline production, including NIR spectroscopy, in-process testing, and real-time release.
Deliver PAT projects and proof-of-concept activities with cross-functional internal and external partners.
Investigate PAT-related issues using root-cause analysis, statistical analysis, and multivariate data analysis.
Support technology transfer, process validation, and the specification, installation, commissioning, and qualification of PAT equipment.
Prepare and review PAT documentation to ensure compliance with standards, policies, SOPs, and applicable safety, health, environmental, and financial requirements.
Deliver PAT training, represent the site in global PAT forums, and support continuous improvement and quality risk management.
Requirements
Master’s degree in science, analytical chemistry, or chemical engineering with applicable experience.
Experience working in an international and multidisciplinary environment.
Flexibility to support reliable production and supply needs.
Knowledge of pharmaceutical production and development technologies.
Nice to have
Working knowledge of chemometrics methodologies.
Working knowledge of current Good Manufacturing Practices (cGMP).
Culture & Benefits
Regular employment with one open position.
Work is based at the Cramlington manufacturing site and involves collaboration with Operations, Quality, Technical functions, and the global PAT network.
hirify.global promotes an inclusive environment and is an equal opportunity employer.
Employees must satisfy applicable travel and credentialing requirements, including associated vaccination prerequisites.
Domestic relocation is listed as available.
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